Substituted benzoycyclohexenones

ABSTRACT

The invention relates to novel substituted benzoylcyclohexenones of the formula (I),  
                 
 
     in which  
     n, A, R 1 , R 2 , R 3 , R 4 , Y and Z are each as defined in the description,  
     and also to processes for their preparation and to their use as herbicides.

[0001] The invention relates to novel substituted benzoylcyclohexenones, to processes for their preparation and to their use as herbicides.

[0002] It is already known that certain substituted benzoylcyclohexanediones have herbicidal properties (cf. EP-A-090 262, EP-A-135 191, EP-A-186 118, EP-A-186 119, EP-A-186 120, EP-A-319 075, WO-A-96/26200, WO-A-97/46530, WO-A-99/07688, WO-A-00/05221). However, the activity of these compounds is not in all respects satisfactory.

[0003] This invention, accordingly, provides the novel substituted benzoylcyclohexenones of the formula (I),

[0004] in which

[0005] n represents the number 0, 1 or 2,

[0006] A represents a single bond or represents alkanediyl (alkylene) having 1 to 6 carbon atoms,

[0007] R¹ represents hydrogen, phenyl or optionally cyano-, halogen-, C₁-C₄-alkoxy- or C₁-C₄-alkylthio-substituted alkyl having 1 to 6 carbon atoms,

[0008] R² represents hydrogen or optionally cyano-, halogen-, C₁-C₄-alkoxy- or C₁-C₄-alkylthio-substituted alkyl having 1 to 6 carbon atoms, or together with R¹ represents alkanediyl (alkylene) having 1 to 6 carbon atoms, or together with R¹—in this case attached to the same carbon atom—and the carbon atom to which R¹ and R² are attached in this case represents a (C═O) grouping,

[0009] R³ represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, halogen, or represents in each case optionally cyano-, halogen- or C₁-C₄-alkoxy-substituted alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, alkylamino, dialkylamino or dialkylaminosulphonyl having in each case 1 to 6 carbon atoms in the alkyl groups,

[0010] R⁴ represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, halogen, or represents in each case optionally cyano-, halogen- or C₁-C₄-alkoxy-substituted alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, alkylamino, dialkylamino or dialkylaminosulphonyl having in each case 1 to 6 carbon atoms in the alkyl groups, and

[0011] Y represents hydrogen, represents optionally cyano-, halogen- or C₁-C₄-alkoxy-substituted alkyl having 1 to 10 carbon atoms, represents in each case optionally cyano-, halogen-, C₁-C₄-alkyl-carbonyl- or C₁-C₄-alkoxy-carbonyl-substituted alkenyl or alkinyl having in each case 2 to 10 carbon atoms, or represents in each case optionally nitro-, amino-, cyano-, carboxyl-, carbamoyl-, thiocarbamoyl-, halogen-, C₁-C₄-alkyl-, C₁-C₄-halogenoalkyl-, C₁-C₄-alkoxy-C₁-C₄-alkyl-, C₁-C₄-alkoxy-, C₁-C₄-halogenoalkoxy-, C₁-C₄-alkylthio-, C₁-C₄-halogenoalkylthio-, C₁-C₄-alkylsulphinyl-, C₁-C₄-halogenoalkylsulphinyl-, C₁-C₄-alkylsulphonyl-, C₁-C₄-halogenoalkylsulphonyl-, C₁-C₄-alkyl-carbonyl-, C₁-C₄-alkoxy-carbonyl-, C₁-C₄-alkyl-carbonyl-amino-, C₁-C₄-alkoxy-carbonyl-amino-, C₁-C₄-alkyl-sulphonyl-amino-substituted aryl or arylalkyl having in each case 6 or 10 carbon atoms in the aryl groups and optionally 1 to 4 carbon atoms in the alkyl moiety, and

[0012] Z represents an optionally substituted 4- to 12-membered saturated or unsaturated, monocyclic or bicyclic, heterocyclic grouping which contains 1 to 4 hetero atoms (up to 4 nitrogen atoms and optionally—alternatively or additionally—one oxygen atom or one sulphur atom, or one SO grouping or one SO₂ grouping), and which contains additionally one to three oxo groups (C═O) and/or thioxo groups (C═S) as components of the heterocycle,

[0013] including all possible tautomeric and, if appropriate, possible stereoisomeric forms of the compounds of the general formula (I), and the possible salts or metal-coordinated derivatives of the compounds of the general formula (I).

[0014] In the definitions, the hydrocarbon chains, such as alkyl or alkanediyl, are in each case straight-chain or branched—including in combination with heteroatoms, such as in alkoxy.

[0015] Preferred meanings of the radicals or groupings present in the formulae shown above and below are defined below.

[0016] n preferably represents the number 0 or 2.

[0017] A preferably represents a single bond or represents alkanediyl (alkylene) having 1 to 4 carbon atoms.

[0018] R¹ preferably represents hydrogen, phenyl or optionally cyano-, halogen-, C₁-C₄-alkoxy- or C₁-C₄-alkylthio-substituted alkyl having 1 to 5 carbon atoms.

[0019] R² preferably represents hydrogen or optionally cyano-, halogen-, C₁-C₄-alkoxy- or C₁-C₄-alkylthio-substituted alkyl having 1 to 5 carbon atoms, or together with R¹ represents alkanediyl (alkylene) having 1 to 5 carbon atoms.

[0020] R³ preferably represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, halogen, or represents in each case optionally cyano-, halogen- or C₁-C₄-alkoxy-substituted alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, alkylamino, dialkylamino or dialkylaminosulphonyl having in each case 1 to 5 carbon atoms in the alkyl groups.

[0021] R⁴ preferably represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, halogen, or represents in each case optionally cyano-, halogen- or C₁-C₄-alkoxy-substituted alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, alkylamino, dialkylamino or dialkylaminosulphonyl having in each case 1 to 5 carbon atoms in the alkyl groups.

[0022] Y preferably represents hydrogen, represents optionally cyano-, halogen- or C₁-C₄-alkoxy-substituted alkyl having 1 to 6 carbon atoms, represents in each case optionally cyano-, halogen-, C₁-C₄-alkyl-carbonyl- or C₁-C₄-alkoxy-carbonyl-substituted alkenyl or alkinyl having in each case 2 to 6 carbon atoms, or represents in each case optionally nitro-, amino-, cyano-, carboxyl-, carbamoyl-, thiocarbamoyl-, halogen-, C₁-C₄-alkyl-, C₁-C₄-halogenoalkyl-, C₁-C₄-alkoxy-C₁-C₄-alkyl-, C₁-C₄-alkoxy-, C₁-C₄-halogenoalkoxy-, C₁-C₄-alkylthio, C₁-C₄-halogenoalkylthio-, C₁-C₄-alkylsulphinyl-, C₁-C₄-halogenoalkylsulphinyl-, C₁-C₄-alkylsulphonyl-, C₁-C₄-halogenoalkylsulphonyl-, C₁-C₄-alkyl-carbonyl-, C₁-C₄-alkoxy-carbonyl-, C₁-C₄-alkyl-carbonyl-amino-, C₁-C₄-alkoxy-carbonyl-amino-, C₁-C₄-alkyl-sulphonyl-amino-substituted aryl or arylalkyl having in each case 6 or 10 carbon atoms in the aryl groups and optionally 1 to 4 carbon atoms in the alkyl moiety.

[0023] Z preferably represents one of the heterocyclic groupings below

[0024] in which the bond drawn broken in each case denotes a single bond or a double bond, and in which each heterocycle preferably only carries two substituents of the definition R⁵ and/or R⁶ in any combination.

[0025] Q represents oxygen or sulphur,

[0026] R⁵ represents hydrogen, hydroxyl, mercapto, cyano, halogen, represents in each case optionally cyano-, halogen-, C₁-C₄-alkoxy-, C₁-C₄-alkylthio-, C₁-C₄-alkylsulphinyl- or C₁-C₄-alkylsulphonyl-substituted alkyl, alkylcarbonyl, alkoxy, alkoxycarbonyl, alkylthio, alkylsulphinyl or alkylsulphonyl having in each case up to 6 carbon atoms in the alkyl groups, represents in each case optionally halogen-substituted alkylamino or dialkylamino having in each case up to 6 carbon atoms in the alkyl groups, represents in each case optionally halogen-substituted alkenyl, alkinyl, alkenyloxy, alkenylthio, alkinylthio or alkenylamino having in each case up to 6 carbon atoms in the alkenyl or alkinyl groups, represents in each case optionally halogen-substituted cycloalkyl, cycloalkyloxy, cycloalkylthio, cycloalkylamino, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkylthio or cycloalkylalkylamino having in each case 3 to 6 carbon atoms in the cycloalkyl groups and optionally up to 4 carbon atoms in the alkyl moiety, or represents in each case optionally halogen-, C₁-C₄-alkyl- or C₁-C₄-alkoxy-substituted phenyl, phenyloxy, phenylthio, phenylamino, benzyl, benzyloxy, benzylthio or benzylamino, represents pyrrolidino, piperidino or morpholino, or—if two adjacent radicals R⁵ and R⁵ are located at a double bond—also together with the adjacent radical R⁵ represents a benzo grouping, and

[0027] R⁶ represents hydrogen, hydroxyl, amino, alkylideneamino having up to 4 carbon atoms, represents in each case optionally halogen- or C₁-C₄-alkoxy-substituted alkyl, alkoxy, alkylamino, dialkylamino or alkanoylamino having in each case up to 6 carbon atoms in the alkyl groups, represents in each case optionally halogen-substituted alkenyl, alkinyl or alkenyloxy having in each case up to 6 carbon atoms in the alkenyl or alkinyl groups, represents in each case optionally halogen-substituted cycloalkyl, cycloalkylalkyl or cycloalkylamino having in each case 3 to 6 carbon atoms in the cycloalkyl groups and optionally up to 3 carbon atoms in the alkyl moiety, or represents in each case optionally halogen-, C₁-C₄-alkyl- or C₁-C₄-alkoxy-substituted phenyl or benzyl, or together with an adjacent radical R⁵ or R⁶ represents optionally halogen- or C₁-C₄-alkyl-substituted alkanediyl having 3 to 5 carbon atoms,

[0028] where the individual radicals R⁵ and R⁶—if two or more of them are attached to the same heterocyclic groupings—may have identical or different meanings in the context of the above definition.

[0029] n particularly preferably represents the number 0.

[0030] A particularly preferably represents a single bond or represents methylene, ethylidene (ethane-1,1-diyl) or dimethylene (ethane-1,2-diyl).

[0031] R¹ particularly preferably represents hydrogen, phenyl or in each case optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-, methylthio-, ethylthio-, n- or i-propylthio-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-butyl.

[0032] R² particularly preferably represents hydrogen or represents in each case optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-, methylthio-, ethylthio-, n- or i-propylthio-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, or together with R¹ represents methylene, ethylidene (ethane-1,1-diyl), dimethylene (ethane-1,2-diyl), propylidene (propane-1,1-diyl) or trimethylene (propane-1,3-diyl).

[0033] R³ particularly preferably represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, fluorine, chlorine, bromine, iodine, or represents in each case optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methylthio, ethylthio, n- or i-propylthio, n-, i-, s- or t-butylthio, methylsulphinyl, ethylsulphinyl, n- or i-propylsulphinyl, methylsulphonyl, ethylsulphonyl, n- or i-propylsulphonyl, methylamino, ethylamino, n- or i-propylamino, n-, i-, s- or t-butylamino, dimethylamino, diethylamino, dimethylaminosulphonyl or diethylaminosulphonyl.

[0034] R⁴ particularly preferably represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, fluorine, chlorine, bromine, iodine, or represents in each case optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methylthio, ethylthio, n- or i-propylthio, n-, i-, s- or t-butylthio, methylsulphinyl, ethylsulphinyl, n- or i-propylsulphinyl, methylsulphonyl, ethylsulphonyl, n- or i-propylsulphonyl, methylamino, ethylamino, n- or i-propylamino, n-, i-, s- or t-butylamino, dimethylamino, diethylamino, dimethylaminosulphonyl or diethylaminosulphonyl.

[0035] Y particularly preferably represents hydrogen, represents in each case optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, represents in each case optionally cyano-, fluorine-, chlorine-, bromine-, acetyl-, propionyl-, n- or i-butyroyl-, methoxycarbonyl-, ethoxycarbonyl-, n- or i-propoxycarbonyl-substituted ethenyl, propenyl, butenyl, pentenyl, ethinyl, propinyl or butinyl, or represents in each case optionally nitro-, amino-, cyano-, carboxyl-, carbamoyl-, thiocarbamoyl-, fluorine-, chlorine-, bromine-, iodine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-, trifluoromethyl-, methoxymethyl-, ethoxymethyl-, methoxyethyl-, ethoxyethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s- or t-butoxy-, difluoromethoxy-, trifluoromethoxy-, methylthio-, ethylthio-, n- or i-propylthio-, n-, i-, s- or t-butylthio-, difluoromethylthio-, trifluoromethylthio-, methylsulphinyl-, ethylsulphinyl-, trifluoromethylsulphinyl-, methylsulphonyl-, ethylsulphonyl-, trifluoromethylsulphonyl-, acetyl-, propionyl-, n- or i-butyroyl-, methoxycarbonyl-, ethoxycarbonyl-, n- or i-propoxycarbonyl-, acetylamino-, propionylamino-, methoxycarbonylamino-, ethoxycarbonylamino-, methylsulphonylamino-, ethylsulphonylamino-, n- or i-propylsulphonylamino-substituted phenyl, naphthyl, benzyl or phenylethyl.

[0036] Z particularly preferably represents one of the heterocyclic groupings below

[0037] Q preferably represents oxygen,

[0038] R⁵ preferably represents hydrogen, hydroxyl, mercapto, cyano, fluorine, chlorine, bromine, iodine, represents in each case optionally fluorine-, chlorine-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s- or t-butoxy-, methylthio-, ethylthio-, n- or i-propylthio-, n-, i-, s- or t-butylthio-, methylsulphinyl-, ethylsulphinyl-, n- or i-propylsulphinyl-, methylsulphonyl-, ethylsulphonyl-, n- or i-propylsulphonyl-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methylthio, ethylthio, n- or i-propylthio, n-, i-, s- or t-butylthio, methylsulphinyl, ethylsulphinyl, n- or i-propylsulphinyl, methylsulphonyl, ethylsulphonyl, n- or i-propylsulphonyl, represents methylamino, ethylamino, n- or i-propylamino, n-, i-, s- or t-butylamino, dimethylamino, diethylamino, di-n-propylamino or di-i-propylamino, represents in each case optionally fluorine- and/or chlorine-substituted ethenyl, propenyl, butenyl, ethinyl, propinyl, butinyl, propenyloxy, butenyloxy, propenylthio, butenylthio, propenylamino or butenylamino, represents in each case optionally fluorine- and/or chlorine-substituted cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cyclopropylthio, cyclobutylthio, cyclopentylthio, cyclohexylthio, cyclopropylamino, cyclobutylamino, cyclopentylamino, cyclohexylamino, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, cyclopropylmethoxy, cyclobutylmethoxy, cyclopentylmethoxy, cyclohexylmethoxy, cyclopropylmethylthio, cyclobutylmethylthio, cyclopentylmethylthio, cyclohexylmethylthio, cyclopropylmethylamino, cyclobutylmethylamino, cyclopentylmethylamino or cyclohexylmethylamino, or represents in each case optionally fluorine-, chlorine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-, methoxy-, ethoxy-, n- or i-propoxy-substituted phenyl, phenyloxy, phenylthio, phenylamino, benzyl, benzyloxy, benzylthio or benzylamino, or—in the case that two adjacent radicals R⁵ and R⁵ are located at a double bond—together with the adjacent radical R⁵ also represents a benzo grouping.

[0039] R⁶ preferably represents hydrogen, hydroxyl, amino, represents in each case optionally fluorine- and/or chlorine-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, methoxy, ethoxy, n- or i-propoxy, methylamino, ethylamino or dimethylamino, represents in each case optionally fluorine- and/or chlorine-substituted ethenyl, propenyl, ethinyl, propinyl or propenyloxy, represented in each case optionally fluorine- and/or chlorine-substituted cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl or cyclohexylmethyl, or represents in each case optionally fluorine-, chlorine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-, methoxy-, ethoxy-, n- or i-propoxy-substituted phenyl or benzyl, or together with an adjacent radical R⁵ or R⁶ represents in each case optionally methyl- and/or ethyl-substituted propane-1,3-diyl (trimethylene), butane-1,4-diyl (tetramethylene) or pentane-1,5-diyl (pentamethylene).

[0040] A very particularly preferably represents a single bond or represents methylene.

[0041] R¹ very particularly preferably represents hydrogen, phenyl or in each case optionally fluorine- or chlorine-substituted methyl, ethyl, n- or i-propyl.

[0042] R² very particularly preferably represents hydrogen or in each case optionally fluorine- or chlorine-substituted methyl, ethyl, n- or i-propyl, or together with R¹ represents methylene or dimethylene.

[0043] R³ very particularly preferably represents hydrogen, nitro, cyano, fluorine, chlorine, bromine, iodine, or represents in each case optionally fluorine-, chlorine-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, methoxy, ethoxy, methylthio, ethylthio, methylsulphinyl, ethylsulphinyl, methylsulphonyl, ethylsulphonyl, methylamino, ethylamino, dimethylamino or dimethylaminosulphonyl.

[0044] R⁴ very particularly preferably represents hydrogen, nitro, cyano, fluorine, chlorine, bromine, iodine, or represents in each case optionally fluorine-, chlorine-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, methoxy, ethoxy, methylthio, ethylthio, methylsulphinyl, ethylsulphinyl, methylsulphonyl, ethylsulphonyl, methylamino, ethylamino, dimethylamino or dimethylaminosulphonyl.

[0045] Y very particularly preferably represents hydrogen, represents in each case optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, represents in each case optionally fluorine-, chlorine- or bromine-substituted propenyl, butenyl, pentenyl, propinyl or butinyl, or represents in each case optionally nitro-, amino-, cyano-, fluorine-, chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-, trifluoromethyl-, methoxymethyl-, ethoxymethyl-, methoxyethyl-, ethoxyethyl-, methoxy-, ethoxy-, n- or i-propoxy-, difluoromethoxy-, trifluoromethoxy-, methylthio-, ethylthio-, n- or i-propylthio-, difluoromethylthio-, trifluoromethylthio-, methylsulphinyl-, ethylsulphinyl-, trifluoromethylsulphinyl-, methylsulphonyl, ethylsulphonyl-, trifluoromethylsulphonyl-, acetyl-, propionyl-, methoxycarbonyl-, ethoxycarbonyl-, acetylamino-, propionylamino-, methoxycarbonylamino-, ethoxycarbonylamino-, methylsulphonylamino- or ethylsulphonylamino-substituted phenyl or benzyl.

[0046] Z very particularly preferably represents the heterocyclic groupings below

[0047] R⁵ particularly preferably represents hydrogen, fluorine, chlorine, bromine, represents in each case optionally fluorine-, chlorine-, methoxy-, ethoxy-, n- or i-propoxy-, methylthio-, ethylthio-, methylsulphinyl-, ethylsulphinyl-, methylsulphonyl-, ethylsulphonyl-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, methoxy, ethoxy, n- or i-propoxy, n-, i- or s-butoxy, methylthio, ethylthio, n- or i-propylthio, n-, 1- or s-butylthio, methylsulphinyl, ethylsulphinyl, n- or i-propylsulphinyl, methylsulphonyl, ethylsulphonyl, n- or i-propylsulphonyl, represents methylamino, ethylamino, n- or i-propylamino, n-, i- or s-butylamino, dimethylamino or diethylamino, represents in each case optionally fluorine- and/or chlorine-substituted ethenyl, propenyl, butenyl, ethinyl, propinyl, butinyl, propenyloxy, butenyloxy, propenylthio or represents in each case optionally fluorine- and/or chlorine-substituted cyclopropyl, cyclopropyloxy, cyclopropylthio, cyclopropylamino, cyclopropylmethyl, cyclopropylmethoxy, cyclopropylmethylthio or cyclopropylmethylamino.

[0048] R⁶ particularly preferably represents hydrogen, represents amino, represents in each case optionally fluorine- and/or chlorine-, methoxy- or ethoxy-substituted methyl, ethyl, methoxy, ethoxy, methylamino or ethylamino, represents dimethylamino, or represents in each case optionally fluorine- and/or chlorine-substituted cyclopropyl, cyclopropylmethyl, phenyl or benzyl, or together with an adjacent radical R⁵ or R⁶ represents in each case optionally methyl- and/or ethyl-substituted propane-1,3-diyl (trimethylene), butane-1,4-diyl (tetramethylene) or pentane-1,5-diyl (pentamethylene).

[0049] A most preferably represents methylene.

[0050] R¹ most preferably represents hydrogen.

[0051] R² most preferably represents hydrogen.

[0052] R³ most preferably represents chlorine, trifluoromethyl or methoxy.

[0053] R⁴ most preferably represents chlorine, trifluoromethyl or methylsulphonyl.

[0054] Y most preferably represents hydrogen, represents in each case optionally fluorine-, chlorine- or methoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, represents in each case optionally fluorine- or chlorine-substituted propenyl, butenyl, pentenyl or represents optionally amino-, cyano-, fluorine-, chlorine-, methyl-, ethyl-, trifluoromethyl-, methoxy- or ethoxy-substituted phenyl.

[0055] R⁵ very particularly preferably represents hydrogen, methyl or ethyl.

[0056] R⁶ very particularly preferably represents hydrogen, methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, cyclopropyl, cyclopropylmethyl, cyclopentyl, cyclopentylmethyl, cyclohexyl, cyclohexylmethyl, phenyl or benzyl.

[0057] R⁵ most preferably represents hydrogen.

[0058] R⁶ most preferably represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, cyclopropyl, cyclopropylmethyl or phenyl.

[0059] The invention preferably also provides the sodium, potassium, magnesium, calcium, ammonium, C₁-C₄-alkyl-ammonium, di-(C₁-C₄-alkyl)-ammonium, tri-(C₁-C₄-alkyl)-ammonium, tetra-(C₁-C₄-alkyl)-ammonium, tri-(C₁-C₄-alkyl)-sulphonium, C₅- or C₆-cycloalkyl-ammonium and di-(C₁-C₂-alkyl)-benzyl-ammonium salts of compounds of the formula (I), in which A, n, R¹, R², R¹, R⁴, Y and Z are each as defined above, or else complex compounds (coordination compounds) of these compounds with metals such as copper, iron, cobalt, nickel.

[0060] Preference according to the invention is given to compounds of the formula (I) which contain a combination of the meanings mentioned above as being preferred.

[0061] Particular preference according to the invention is given to compounds of the formula (I) which contain a combination of the meanings listed above as being particularly preferred.

[0062] Very particular preference according to the invention is given to compounds of the formula (I) which contain a combination of the meanings listed above as being very particularly preferred.

[0063] Most preference according to the invention is given to compounds of the formula (I) which contain a combination of the meanings listed above as being most preferred.

[0064] The general or preferred radical definitions listed above apply both to the end products of the formula (I) and, correspondingly, to the starting materials or intermediates required in each case for the preparation. These radical definitions can be combined with one another as desired, i.e. including combinations between the given preferred ranges.

[0065] The position of the radicals R¹, R², R³, R⁴ and A-Z can vary according to formula (I).

[0066] The radical R³ is preferably in position (4) on the phenyl ring, particularly preferably in position (2).

[0067] The radical R⁴ is preferably in position (4) on the phenyl ring, if the radical R³ is in position (2).

[0068] The radical A-Z is preferably in position (2) on the phenyl ring, particularly preferably in position (3), and particular preference is given to the substitution pattern (2)-R³, (4)-R⁴ and (3)-A-Z.

[0069] The present invention provides in particular the compounds of the general formulae (IA), (IB) and (IC) below.

[0070] In the general formulae (IA), (IB) and (IC), n, A, R¹, R², R¹, R⁴, Y and Z have in each case the meanings given in the definitions above.

[0071] Very particular emphasis is given to the compounds of the general formulae (IA), (IB) and (IC) in which A represents methylene.

[0072] Examples of compounds of the general formula (I) according to the invention are listed in the groups below.

[0073] Group 1

[0074] Here, R³, R⁴, R⁵ and R⁶ each have, for example, the meanings given in the table below: (position) R³ R⁴ R⁵ R⁶ H — CF₃ CH₃ F — CF₃ CH₃ Cl — CF₃ CH₃ Br — CF₃ CH₃ I — CF₃ CH₃ NO₂ — CF₃ CH₃ CN — CF₃ CH₃ CH₃ — CF₃ CH₃ OCH₃ — CF₃ CH₃ CF₃ — CF₃ CH₃ OCHF₂ — CF₃ CH₃ OCF₃ — CF₃ CH₃ SO₂CH₃ — CF₃ CH₃ H — OCH₃ CH₃ F — OCH₃ CH₃ Cl — OCH₃ CH₃ Br — OCH₃ CH₃ I — OCH₃ CH₃ NO₂ — OCH₃ CH₃ CN — OCH₃ CH₃ CH₃ — OCH₃ CH₃ OCH₃ — OCH₃ CH₃ CF₃ — OCH₃ CH₃ OCHF₂ — OCH₃ CH₃ OCF₃ — OCH₃ CH₃ SO₂CH₃ — OCH₃ CH₃ H — SCH₃ CH₃ F — SCH₃ CH₃ Cl — SCH₃ CH₃ Br — SCH₃ CH₃ I — SCH₃ CH₃ NO₂ — SCH₃ CH₃ CN — SCH₃ CH₃ CH₃ — SCH₃ CH₃ OCH₃ — SCH₃ CH₃ CF₃ — SCH₃ CH₃ OCHF₂ — SCH₃ CH₃ OCF₃ — SCH₃ CH₃ SO₂CH₃ — SCH₃ CH₃ H — OC₂H₅ CH₃ F — OC₂H₅ CH₃ Cl — OC₂H₅ CH₃ Br — OC₂H₅ CH₃ I — OC₂H₅ CH₃ NO₂ — OC₂H₅ CH₃ CN — OC₂H₅ CH₃ CH₃ — OC₂H₅ CH₃ OCH₃ — OC₂H₅ CH₃ CF₃ — OC₂H₅ CH₃ OCHF₂ — OC₂H₅ CH₃ OCF₃ — OC₂H₅ CH₃ SO₂CH₃ — OC₂H₅ CH₃ H — N(CH₃)₂ CH₃ F — N(CH₃)₂ CH₃ Cl — N(CH₃)₂ CH₃ Br — N(CH₃)₂ CH₃ I — N(CH₃)₂ CH₃ NO₂ — N(CH₃)₂ CH₃ CN — N(CH₃)₂ CH₃ CH₃ — N(CH₃)₂ CH₃ OCH₃ — N(CH₃)₂ CH₃ CF₃ — N(CH₃)₂ CH₃ OCHF₂ — N(CH₃)₂ CH₃ OCF₃ — N(CH₃)₂ CH₃ SO₂CH₃ — N(CH₃)₂ CH₃ H — OCH₃

F — OCH₃

Cl — OCH₃

Br — OCH₃

I — OCH₃

NO₂ — OCH₃

CN — OCH₃

CH₃ — OCH₃

OCH₃ — OCH₃

CF₃ — OCH₃

OCHF₂ — OCH₃

OCF₃ — OCH₃

SO₂CH₃ — OCH₃

H (3-) Cl CF₃ CH₃ F (3-) Cl CH₃ CH₃ Cl (3-) Cl OCH₃ CH₃ Br (3-) Cl Br

Cl (3-) Cl CF₃ CH₃ NO₂ (3-) Cl CH₃ CH₃ Cl (3-) Cl SCH₃ CH₃ CH₃ (3-) Cl Cl CH₃ OCH₃ (3-) Cl OCH₃ CH₃ CF₃ (3-) Cl CF₃ CH₃ OCHF₂ (3-) Cl CH₃ CH₃ OCF₃ (3-) Cl CH₃ CH₃ SO₂CH₃ (3-) Cl OCH₃ CH₃ F — C₂H₅ OCH₃ Cl — C₂H₅ OCH₃ Br — C₂H₅ OCH₃ CF₃ — C₂H₅ OCH₃ SO₂CH₃ — C₂H₅ OCH₃ F — C₂H₅ C₂H₅ Cl — C₂H₅ C₂H₅ Br — C₂H₅ C₂H₅ CF₃ — C₂H₅ C₂H₅ SO₂CH₃ — C₂H₅ C₂H₅

[0075] Group 2

[0076] Here, R³, R⁴, R⁵ and R each have, for example, the meanings given above in Group 1.

[0077] Group 3

[0078] Here, R³, R⁴, R⁵ and R⁶ each have, for example, the meanings given above in Group 1.

[0079] Group 4

[0080] Here, R³, R⁴, R⁵ and R⁶ each have, for example, the meanings given above in Group 1.

[0081] Group 5

[0082] Here, R³, R⁴, R⁵ and R⁶ each have, for example, the meanings given above in Group 1.

[0083] Group 6

[0084] Here, R³, R⁴, R⁵ and R⁶ each have, for example, the meanings given above in the table below. (position) R³ R⁴ R⁵ R⁶ Cl (2-) Cl CF₃ CH₃ Cl (2-) Cl SCH₃ CH₃ Cl (2-) Cl SC₂H₅ CH₃ Cl (2-) Cl SC₃H₇ CH₃ Cl (2-) Cl SC₃H₇-i CH₃ Cl (2-) Cl

CH₃ Cl (2-) Cl

CH₃ Cl (2-) Cl

CH₃ Cl (2-) Cl

CH₃ Cl (2-) Cl

CH₃ Cl (2-) Cl SCH═C═CH₂ CH₃ Cl (2-) Cl SCH₂CN CH₃ Cl (2-) Cl SCH₂CH₂CN CH₃ Cl (2-) Cl OCH₃ CH₃ Cl (2-) Cl OC₂H₅ CH₃ Cl (2-) Cl OC₃H₇ CH₃ Cl (2-) Cl OC₃H₇-i CH₃ Cl (2-) Cl OC₄H₉ CH₃ Cl (2-) Cl OCH₂CF₃ CH₃ Cl (2-) Cl

CH₃ Cl (2-) Cl OC₆H₅ CH₃ Cl (2-) Cl H CH₃ Cl (2-) Cl CH₃ CH₃ Cl (2-) Cl C₂H₅ CH₃ Cl (2-) Cl C₃H₇ CH₃ Cl (2-) Cl C₃H₇-i CH₃ Cl (2-) Cl C₄H₉ CH₃ Cl (2-) Cl C₄H₉-i CH₃ Cl (2-) Cl C₄H₉-s CH₃ Cl (2-) Cl C₄H₉-t CH₃ Cl (2-) Cl

CH₃ Cl (2-) Cl

CH₃ Cl (2-) Cl CH═CHCH₃ CH₃ Cl (2-) Cl

CH₃ Cl (2-) Cl

CH₃ Cl (2-) Cl

CH₃ Cl (2-) Cl N(CH₃)₂ CH₃ Cl (2-) Cl

CH₃ Cl (2-) Cl Cl CH₃ Cl (2-) Cl Br CH₃ SO₂CH₃ (2-) Cl CF₃ CH₃ SO₂CH₃ (2-) Cl SCH₃ CH₃ SO₂CH₃ (2-) Cl SC₂H₅ CH₃ SO₂CH₃ (2-) Cl SC₃H₇ CH₃ SO₂CH₃ (2-) Cl SC₃H₇-i CH₃ SO₂CH₃ (2-) Cl

CH₃ SO₂CH₃ (2-) Cl

CH₃ SO₂CH₃ (2-) Cl

CH₃ SO₂CH₃ (2-) Cl

CH₃ SO₂CH₃ (2-) Cl

CH₃ SO₂CH₃ (2-) Cl SCH═C═CH₂ CH₃ SO₂CH₃ (2-) Cl SCH₂CN CH₃ SO₂CH₃ (2-) Cl SCH₂CH₂CN CH₃ SO₂CH₃ (2-) Cl OCH₃ CH₃ SO₂CH₃ (2-) Cl OC₂H₅ CH₃ SO₂CH₃ (2-) Cl OC₃H₇ CH₃ SO₂CH₃ (2-) Cl OC₃H₇-i CH₃ SO₂CH₃ (2-) Cl OC₄H₉ CH₃ SO₂CH₃ (2-) Cl OCH₂CF₃ CH₃ SO₂CH₃ (2-) Cl

CH₃ SO₂CH₃ (2-) Cl OC₆H₅ CH₃ SO₂CH₃ (2-) Cl H CH₃ SO₂CH₃ (2-) Cl CH₃ CH₃ SO₂CH₃ (2-) Cl C₂H₅ CH₃ SO₂CH₃ (2-) Cl C₃H₇ CH₃ SO₂CH₃ (2-) Cl C₃H₇-i CH₃ SO₂CH₃ (2-) Cl C₄H₉ CH₃ SO₂CH₃ (2-) Cl C₄H₉-i CH₃ SO₂CH₃ (2-) Cl C₄H₉-s CH₃ SO₂CH₃ (2-) Cl C₄H₉-t CH₃ SO₂CH₃ (2-) Cl

CH₃ SO₂CH₃ (2-) Cl

CH₃ SO₂CH₃ (2-) Cl CH═CHCH₃ CH₃ SO₂CH₃ (2-) Cl

CH₃ SO₂CH₃ (2-) Cl

CH₃ SO₂CH₃ (2-) Cl

CH₃ SO₂CH₃ (2-) Cl N(CH₃)₂ CH₃ SO₂CH₃ (2-) Cl

CH₃ SO₂CH₃ (2-) Cl Cl CH₃ SO₂CH₃ (2-) Cl Br CH₃ Cl (2-) SO₂CH₃ CF₃ CH₃ Cl (2-) SO₂CH₃ SCH₃ CH₃ Cl (2-) SO₂CH₃ SC₂H₅ CH₃ Cl (2-) SO₂CH₃ SC₃H₇ CH₃ Cl (2-) SO₂CH₃ SC₃H₇-i CH₃ Cl (2-) SO₂CH₃

CH₃ Cl (2-) SO₂CH₃

CH₃ Cl (2-) SO₂CH₃

CH₃ Cl (2-) SO₂CH₃

CH₃ Cl (2-) SO₂CH₃

CH₃ Cl (2-) SO₂CH₃ SCH═C═CH₂ CH₃ Cl (2-) SO₂CH₃ SCH₂CN CH₃ Cl (2-) SO₂CH₃ SCH₂CH₂CN CH₃ Cl (2-) SO₂CH₃ OCH₃ CH₃ Cl (2-) SO₂CH₃ OC₂H₅ CH₃ Cl (2-) SO₂CH₃ OC₃H₇ CH₃ Cl (2-) SO₂CH₃ OC₃H₇-i CH₃ Cl (2-) SO₂CH₃ OC₄H₉ CH₃ Cl (2-) SO₂CH₃ OCH₂CF₃ CH₃ Cl (2-) SO₂CH₃

CH₃ Cl (2-) SO₂CH₃ OC₆H₅ CH₃ Cl (2-) SO₂CH₃ H CH₃ Cl (2-) SO₂CH₃ CH₃ CH₃ Cl (2-) SO₂CH₃ C₂H₅ CH₃ Cl (2-) SO₂CH₃ C₃H₇ CH₃ Cl (2-) SO₂CH₃ C₃H₇-i CH₃ Cl (2-) SO₂CH₃ C₄H₉ CH₃ Cl (2-) SO₂CH₃ C₄H₉-i CH₃ Cl (2-) SO₂CH₃ C₄H₉-s CH₃ Cl (2-) SO₂CH₃ C₄H₉-t CH₃ Cl (2-) SO₂CH₃

CH₃ Cl (2-) SO₂CH₃

CH₃ Cl (2-) SO₂CH₃ CH═CHCH₃ CH₃ Cl (2-) SO₂CH₃

CH₃ Cl (2-) SO₂CH₃

CH₃ Cl (2-) SO₂CH₃

CH₃ Cl (2-) SO₂CH₃ N(CH₃)₂ CH₃ Cl (2-) SO₂CH₃

CH₃ Cl (2-) SO₂CH₃ Cl CH₃ Cl (2-) SO₂CH₃ Br CH₃ Cl (2-) Cl CF₃

Cl (2-) Cl SCH₃

Cl (2-) Cl SC₂H₅

Cl (2-) Cl SC₃H₇

Cl (2-) Cl SC₃H₇-i

Cl (2-) Cl

Cl (2-) Cl

Cl (2-) Cl

Cl (2-) Cl

Cl (2-) Cl

Cl (2-) Cl SCH═C═CH₂

Cl (2-) Cl SCH₂CN

Cl (2-) Cl SCH₂CH₂CN

Cl (2-) Cl OCH₃

Cl (2-) Cl OC₂H₅

Cl (2-) Cl OC₃H₇

Cl (2-) Cl OC₃H₇-i

Cl (2-) Cl OC₄H₉

Cl (2-) Cl OCH₂CF₃

Cl (2-) Cl

Cl (2-) Cl OC₆H₅

Cl (2-) Cl H

Cl (2-) Cl CH₃

Cl (2-) Cl C₂H₅

Cl (2-) Cl C₃H₇

Cl (2-) Cl C₃H₇-i

Cl (2-) Cl C₄H₉

Cl (2-) Cl C₄H₉-i

Cl (2-) Cl C₄H₉-s

Cl (2-) Cl C₄H₉-t

Cl (2-) Cl

Cl (2-) Cl

Cl (2-) Cl CH═CHCH₃

Cl (2-) Cl

Cl (2-) Cl

Cl (2-) Cl

Cl (2-) Cl N(CH₃)₂

Cl (2-) Cl

Cl (2-) Cl Cl

Cl (2-) Cl Br

SO₂CH₃ (2-) Cl CF₃

SO₂CH₃ (2-) Cl SCH₃

SO₂CH₃ (2-) Cl SC₂H₅

SO₂CH₃ (2-) Cl SC₃H₇

SO₂CH₃ (2-) Cl SC₃H₇-i

SO₂CH₃ (2-) Cl

SO₂CH₃ (2-) Cl

SO₂CH₃ (2-) Cl

SO₂CH₃ (2-) Cl

SO₂CH₃ (2-) Cl

SO₂CH₃ (2-) Cl SCH═C═CH₂

SO₂CH₃ (2-) Cl SCH₂CN

SO₂CH₃ (2-) Cl SCH₂CH₂CN

SO₂CH₃ (2-) Cl OCH₃

SO₂CH₃ (2-) Cl OC₂H₅

SO₂CH₃ (2-) Cl OC₃H₇

SO₂CH₃ (2-) Cl OC₃H₇-i

SO₂CH₃ (2-) Cl OC₄H₉

SO₂CH₃ (2-) Cl OCH₂CF₃

SO₂CH₃ (2-) Cl

SO₂CH₃ (2-) Cl OC₆H₅

SO₂CH₃ (2-) Cl H

SO₂CH₃ (2-) Cl CH₃

SO₂CH₃ (2-) Cl C₂H₅

SO₂CH₃ (2-) Cl C₃H₇

SO₂CH₃ (2-) Cl C₃H₇-i

SO₂CH₃ (2-) Cl C₄H₉

SO₂CH₃ (2-) Cl C₄H₉-i

SO₂CH₃ (2-) Cl C₄H₉-s

SO₂CH₃ (2-) Cl C₄H₉-t

SO₂CH₃ (2-) Cl

SO₂CH₃ (2-) Cl

SO₂CH₃ (2-) Cl CH═CHCH₃

SO₂CH₃ (2-) Cl

SO₂CH₃ (2-) Cl

SO₂CH₃ (2-) Cl

SO₂CH₃ (2-) Cl N(CH₃)₂

SO₂CH₃ (2-) Cl

SO₂CH₃ (2-) Cl Cl

SO₂CH₃ (2-) Cl Br

Cl (2-) SO₂CH₃ CF₃

Cl (2-) SO₂CH₃ SCH₃

Cl (2-) SO₂CH₃ SC₂H₅

Cl (2-) SO₂CH₃ SC₃H₇

Cl (2-) SO₂CH₃ SC₃H₇-i

Cl (2-) SO₂CH₃

Cl (2-) SO₂CH₃

Cl (2-) SO₂CH₃

Cl (2-) SO₂CH₃

Cl (2-) SO₂CH₃

Cl (2-) SO₂CH₃ SCH═C═CH₂

Cl (2-) SO₂CH₃ SCH₂CN

Cl (2-) SO₂CH₃ SCH₂CH₂CN

Cl (2-) SO₂CH₃ OCH₃

Cl (2-) SO₂CH₃ OC₂H₅

Cl (2-) SO₂CH₃ OC₃H₇

Cl (2-) SO₂CH₃ OC₃H₇-i

Cl (2-) SO₂CH₃ OC₄H₉

Cl (2-) SO₂CH₃ OCH₂CF₃

Cl (2-) SO₂CH₃

Cl (2-) SO₂CH₃ OC₆H₅

Cl (2-) SO₂CH₃ H

Cl (2-) SO₂CH₃ CH₃

Cl (2-) SO₂CH₃ C₂H₅

Cl (2-) SO₂CH₃ C₃H₇

Cl (2-) SO₂CH₃ C₃H₇-i

Cl (2-) SO₂CH₃ C₄H₉

Cl (2-) SO₂CH₃ C₄H₉-i

Cl (2-) SO₂CH₃ C₄H₉-s

Cl (2-) SO₂CH₃ C₄H₉-t

Cl (2-) SO₂CH₃

Cl (2-) SO₂CH₃

Cl (2-) SO₂CH₃ CH═CHCH₃

Cl (2-) SO₂CH₃

Cl (2-) SO₂CH₃

Cl (2-) SO₂CH₃

Cl (2-) SO₂CH₃ N(CH₃)₂

Cl (2-) SO₂CH₃

Cl (2-) SO₂CH₃ Cl

Cl (2-) SO₂CH₃ Br

Cl (2-) Cl CF₃ N(CH₃)₂ Cl (2-) Cl SCH₃ N(CH₃)₂ Cl (2-) Cl SC₂H₅ N(CH₃)₂ Cl (2-) Cl SC₃H₇ N(CH₃)₂ Cl (2-) Cl SC₃H₇-i N(CH₃)₂ Cl (2-) Cl

N(CH₃)₂ Cl (2-) Cl

N(CH₃)₂ Cl (2-) Cl

N(CH₃)₂ Cl (2-) Cl

N(CH₃)₂ Cl (2-) Cl

N(CH₃)₂ Cl (2-) Cl SCH═C═CH₂ N(CH₃)₂ Cl (2-) Cl SCH₂CN N(CH₃)₂ Cl (2-) Cl SCH₂CH₂CN N(CH₃)₂ Cl (2-) Cl OCH₃ N(CH₃)₂ Cl (2-) Cl OC₂H₅ N(CH₃)₂ Cl (2-) Cl OC₃H₇ N(CH₃)₂ Cl (2-) Cl OC₃H₇-i N(CH₃)₂ Cl (2-) Cl OC₄H₉ N(CH₃)₂ Cl (2-) Cl OCH₂CF₃ N(CH₃)₂ Cl (2-) Cl

N(CH₃)₂ Cl (2-) Cl OC₆H₅ N(CH₃)₂ Cl (2-) Cl H N(CH₃)₂ Cl (2-) Cl CH₃ N(CH₃)₂ Cl (2-) Cl C₂H₅ N(CH₃)₂ Cl (2-) Cl C₃H₇ N(CH₃)₂ Cl (2-) Cl C₃H₇-i N(CH₃)₂ Cl (2-) Cl C₄H₉ N(CH₃)₂ Cl (2-) Cl C₄H₉-i N(CH₃)₂ Cl (2-) Cl C₄H₉-s N(CH₃)₂ Cl (2-) Cl C₄H₉-t N(CH₃)₂ Cl (2-) Cl

N(CH₃)₂ Cl (2-) Cl

N(CH₃)₂ Cl (2-) Cl CH═CHCH₃ N(CH₃)₂ Cl (2-) Cl

N(CH₃)₂ Cl (2-) Cl

N(CH₃)₂ Cl (2-) Cl

N(CH₃)₂ Cl (2-) Cl N(CH₃)₂ N(CH₃)₂ Cl (2-) Cl

N(CH₃)₂ Cl (2-) Cl Cl N(CH₃)₂ Cl (2-) Cl Br N(CH₃)₂ SO₂CH₃ (2-) Cl CF₃ N(CH₃)₂ SO₂CH₃ (2-) Cl SCH₃ N(CH₃)₂ SO₂CH₃ (2-) Cl SC₂H₅ N(CH₃)₂ SO₂CH₃ (2-) Cl SC₃H₇ N(CH₃)₂ SO₂CH₃ (2-) Cl SC₃H₇-i N(CH₃)₂ SO₂CH₃ (2-) Cl

N(CH₃)₂ SO₂CH₃ (2-) Cl

N(CH₃)₂ SO₂CH₃ (2-) Cl

N(CH₃)₂ SO₂CH₃ (2-) Cl

N(CH₃)₂ SO₂CH₃ (2-) Cl

N(CH₃)₂ SO₂CH₃ (2-) Cl SCH═C═CH₂ N(CH₃)₂ SO₂CH₃ (2-) Cl SCH₂CN N(CH₃)₂ SO₂CH₃ (2-) Cl SCH₂CH₂CN N(CH₃)₂ SO₂CH₃ (2-) Cl OCH₃ N(CH₃)₂ SO₂CH₃ (2-) Cl OC₂H₅ N(CH₃)₂ SO₂CH₃ (2-) Cl OC₃H₇ N(CH₃)₂ SO₂CH₃ (2-) Cl OC₃H₇-i N(CH₃)₂ SO₂CH₃ (2-) Cl OC₄H₉ N(CH₃)₂ SO₂CH₃ (2-) Cl OCH₂CF₃ N(CH₃)₂ SO₂CH₃ (2-) Cl

N(CH₃)₂ SO₂CH₃ (2-) Cl OC₆H₅ N(CH₃)₂ SO₂CH₃ (2-) Cl H N(CH₃)₂ SO₂CH₃ (2-) Cl CH₃ N(CH₃)₂ SO₂CH₃ (2-) Cl C₂H₅ N(CH₃)₂ SO₂CH₃ (2-) Cl C₃H₇ N(CH₃)₂ SO₂CH₃ (2-) Cl C₃H₇-i N(CH₃)₂ SO₂CH₃ (2-) Cl C₄H₉ N(CH₃)₂ SO₂CH₃ (2-) Cl C₄H₉-i N(CH₃)₂ SO₂CH₃ (2-) Cl C₄H₉-s N(CH₃)₂ SO₂CH₃ (2-) Cl C₄H₉-t N(CH₃)₂ SO₂CH₃ (2-) Cl

N(CH₃)₂ SO₂CH₃ (2-) Cl

N(CH₃)₂ SO₂CH₃ (2-) Cl CH═CHCH₃ N(CH₃)₂ SO₂CH₃ (2-) Cl

N(CH₃)₂ SO₂CH₃ (2-) Cl

N(CH₃)₂ SO₂CH₃ (2-) Cl

N(CH₃)₂ SO₂CH₃ (2-) Cl N(CH₃)₂ N(CH₃)₂ SO₂CH₃ (2-) Cl

N(CH₃)₂ SO₂CH₃ (2-) Cl Cl N(CH₃)₂ SO₂CH₃ (2-) Cl Br N(CH₃)₂ Cl (2-) SO₂CH₃ CF₃ N(CH₃)₂ Cl (2-) SO₂CH₃ SCH₃ N(CH₃)₂ Cl (2-) SO₂CH₃ SC₂H₅ N(CH₃)₂ Cl (2-) SO₂CH₃ SC₃H₇ N(CH₃)₂ Cl (2-) SO₂CH₃ SC₃H₇-i N(CH₃)₂ Cl (2-) SO₂CH₃

N(CH₃)₂ Cl (2-) SO₂CH₃

N(CH₃)₂ Cl (2-) SO₂CH₃

N(CH₃)₂ Cl (2-) SO₂CH₃

N(CH₃)₂ Cl (2-) SO₂CH₃

N(CH₃)₂ Cl (2-) SO₂CH₃ SCH═C═CH₂ N(CH₃)₂ Cl (2-) SO₂CH₃ SCH₂CN N(CH₃)₂ Cl (2-) SO₂CH₃ SCH₂CH₂CN N(CH₃)₂ Cl (2-) SO₂CH₃ OCH₃ N(CH₃)₂ Cl (2-) SO₂CH₃ OC₂H₅ N(CH₃)₂ Cl (2-) SO₂CH₃ OC₃H₇ N(CH₃)₂ Cl (2-) SO₂CH₃ OC₃H₇-i N(CH₃)₂ Cl (2-) SO₂CH₃ OC₄H₉ N(CH₃)₂ Cl (2-) SO₂CH₃ OCH₂CF₃ N(CH₃)₂ Cl (2-) SO₂CH₃

N(CH₃)₂ Cl (2-) SO₂CH₃ OC₆H₅ N(CH₃)₂ Cl (2-) SO₂CH₃ H N(CH₃)₂ Cl (2-) SO₂CH₃ CH₃ N(CH₃)₂ Cl (2-) SO₂CH₃ C₂H₅ N(CH₃)₂ Cl (2-) SO₂CH₃ C₃H₇ N(CH₃)₂ Cl (2-) SO₂CH₃ C₃H₇-i N(CH₃)₂ Cl (2-) SO₂CH₃ C₄H₉ N(CH₃)₂ Cl (2-) SO₂CH₃ C₄H₉-i N(CH₃)₂ Cl (2-) SO₂CH₃ C₄H₉-s N(CH₃)₂ Cl (2-) SO₂CH₃ C₄H₉-t N(CH₃)₂ Cl (2-) SO₂CH₃

N(CH₃)₂ Cl (2-) SO₂CH₃

N(CH₃)₂ Cl (2-) SO₂CH₃ CH═CHCH₃ N(CH₃)₂ Cl (2-) SO₂CH₃

N(CH₃)₂ Cl (2-) SO₂CH₃

N(CH₃)₂ Cl (2-) SO₂CH₃

N(CH₃)₂ Cl (2-) SO₂CH₃ N(CH₃)₂ N(CH₃)₂ Cl (2-) SO₂CH₃

N(CH₃)₂ Cl (2-) SO₂CH₃ Cl N(CH₃)₂ Cl (2-) SO₂CH₃ Br N(CH₃)₂ Cl (2-) Cl CH₃ OCH₃ Cl (2-) Cl C₂H₅ OCH₃ Cl (2-) Cl C₃H₇ OCH₃ Cl (2-) Cl SCH₃ OCH₃ Cl (2-) Cl SC₂H₅ OCH₃ Cl (2-) Cl OCH₃ OCH₃ Cl (2-) Cl OC₂H₅ OCH₃ Cl (2-) Cl CH₃ OC₂H₅ Cl (2-) Cl C₂H₅ OC₂H₅ Cl (2-) Cl C₃H₇ OC₂H₅ Cl (2-) Cl SCH₃ OC₂H₅ Cl (2-) Cl SC₂H₅ OC₂H₅ Cl (2-) Cl OCH₃ OC₂H₅ Cl (2-) Cl OC₂H₅ OC₂H₅ Cl (2-) SO₂CH₃ CH₃ OCH₃ Cl (2-) SO₂CH₃ C₂H₅ OCH₃ Cl (2-) SO₂CH₃ C₃H₇ OCH₃ Cl (2-) SO₂CH₃ SCH₃ OCH₃ Cl (2-) SO₂CH₃ SC₂H₅ OCH₃ Cl (2-) SO₂CH₃ OCH₃ OCH₃ Cl (2-) SO₂CH₃ OC₂H₅ OCH₃ Cl (2-) SO₂CH₃ CH₃ OC₂H₅ Cl (2-) SO₂CH₃ C₂H₅ OC₂H₅ Cl (2-) SO₂CH₃ C₃H₇ OC₂H₅ Cl (2-) SO₂CH₃ SCH₃ OC₂H₅ Cl (2-) SO₂CH₃ SC₂H₅ OC₂H₅ Cl (2-) SO₂CH₃ OCH₃ OC₂H₅ Cl (2-) SO₂CH₃ OC₂H₅ OC₂H₅ SO₂CH₃ (2-) Cl Cl OCH₃ SO₂CH₃ (2-) Cl Br OCH₃ SO₂CH₃ (2-) Cl CH₃ OCH₃ SO₂CH₃ (2-) Cl C₂H₅ OCH₃ SO₂CH₃ (2-) Cl C₃H₇ OCH₃ SO₂CH₃ (2-) Cl SCH₃ OCH₃ SO₂CH₃ (2-) Cl SC₂H₅ OCH₃ SO₂CH₃ (2-) Cl OCH₃ OC₂H₅ SO₂CH₃ (2-) Cl OC₂H₅ OC₂H₅ SO₂CH₃ (2-) Cl CH₃ OC₂H₅ SO₂CH₃ (2-) Cl C₂H₅ OC₂H₅ SO₂CH₃ (2-) Cl C₃H₇ OC₂H₅ SO₂CH₃ (2-) Cl SCH₃ OC₂H₅ SO₂CH₃ (2-) Cl SC₂H₅ OC₂H₅ SO₂CH₃ (2-) Cl OCH₃ OC₂H₅ CF₃ (2-) Cl Br CH₃ CF₃ (2-) Cl SCH₃ CH₃ CF₃ (2-) Cl OCH₃ CH₃ CF₃ (2-) Cl N(CH₃)₂ CH₃ CF₃ (2-) Cl CF₃ CH₃ CF₃ (2-) NO₂ Br CH₃ CF₃ (2-) NO₂ SCH₃ CH₃ CF₃ (2-) NO₂ OCH₃ CH₃ CF₃ (2-) NO₂ N(CH₃)₂ CH₃ CF₃ (2-) NO₂ CF₃ CH₃ CF₃ (2-) CH₃ Br CH₃ CF₃ (2-) CH₃ SCH₃ CH₃ CF₃ (2-) CH₃ OCH₃ CH₃ CF₃ (2-) CH₃ N(CH₃)₂ CH₃ CF₃ (2-) CH₃ CF₃ CH₃ CF₃ (2-) OCH₃ Br CH₃ CF₃ (2-) OCH₃ SCH₃ CH₃ CF₃ (2-) OCH₃ OCH₃ CH₃ CF₃ (2-) OCH₃ N(CH₃)₂ CH₃ CF₃ (2-) OCH₃ CF₃ CH₃ SO₂CH₃ (2-) NO₂ Br CH₃ SO₂CH₃ (2-) NO₂ SCH₃ CH₃ SO₂CH₃ (2-) NO₂ OCH₃ CH₃ SO₂CH₃ (2-) NO₂ N(CH₃)₂ CH₃ SO₂CH₃ (2-) NO₂ CF₃ CH₃ SO₂CH₃ (2-) CF₃ Br CH₃ SO₂CH₃ (2-) CF₃ SCH₃ CH₃ SO₂CH₃ (2-) CF₃ OCH₃ CH₃ SO₂CH₃ (2-) CF₃ N(CH₃)₂ CH₃ SO₂CH₃ (2-) CF₃ CF₃ CH₃ SO₂CH₃ (2-) SO₂CH₃ Br CH₃ SO₂CH₃ (2-) SO₂CH₃ SCH₃ CH₃ SO₂CH₃ (2-) SO₂CH₃ OCH₃ CH₃ SO₂CH₃ (2-) SO₂CH₃ N(CH₃)₂ CH₃ SO₂CH₃ (2-) SO₂CH₃ CF₃ CH₃ CN (2-) Cl Br CH₃ CN (2-) Cl SCH₃ CH₃ CN (2-) Cl OCH₃ CH₃ CN (2-) Cl N(CH₃)₂ CH₃ CN (2-) Cl CF₃ CH₃ CN (2-) NO₂ Br CH₃ CN (2-) NO₂ SCH₃ CH₃ CN (2-) NO₂ OCH₃ CH₃ CN (2-) NO₂ N(CH₃)₂ CH₃ CN (2-) NO₂ CF₃ CH₃ CN (2-) CF₃ Br CH₃ CN (2-) CF₃ SCH₃ CH₃ CN (2-) CF₃ OCH₃ CH₃ CN (2-) CF₃ N(CH₃)₂ CH₃ CN (2-) CF₃ CF₃ CH₃ CN (2-) SO₂CH₃ Br CH₃ CN (2-) SO₂CH₃ SCH₃ CH₃ CN (2-) SO₂CH₃ OCH₃ CH₃ CN (2-) SO₂CH₃ N(CH₃)₂ CH₃ CN (2-) SO₂CH₃ CF₃ CH₃ Br (2-) NO₂ Br CH₃ Br (2-) NO₂ SCH₃ CH₃ Br (2-) NO₂ OCH₃ CH₃ Br (2-) NO₂ N(CH₃)₂ CH₃ Br (2-) NO₂ CF₃ CH₃ Br (2-) CF₃ Br CH₃ Br (2-) CF₃ SCH₃ CH₃ Br (2-) CF₃ OCH₃ CH₃ Br (2-) CF₃ N(CH₃)₂ CH₃ Br (2-) CF₃ CF₃ CH₃ Br (2-) SO₂CH₃ Br CH₃ Br (2-) SO₂CH₃ SCH₃ CH₃ Br (2-) SO₂CH₃ OCH₃ CH₃ Br (2-) SO₂CH₃ N(CH₃)₂ CH₃ Br (2-) SO₂CH₃ CF₃ CH₃ Br (2-) CH₃ Br CH₃ Br (2-) CH₃ SCH₃ CH₃ Br (2-) CH₃ OCH₃ CH₃ Br (2-) CH₃ N(CH₃)₂ CH₃ Br (2-) CH₃ CF₃ CH₃ Cl (2-) OCH₃ CF₃ CH₃ Cl (2-) OCH₃ SCH₃ CH₃ Cl (2-) OCH₃ SC₂H₅ CH₃ Cl (2-) OCH₃ SC₃H₇ CH₃ Cl (2-) OCH₃ SC₃H₇-i CH₃ Cl (2-) OCH₃

CH₃ Cl (2-) OCH₃

CH₃ Cl (2-) OCH₃

CH₃ Cl (2-) OCH₃

CH₃ Cl (2-) OCH₃

CH₃ Cl (2-) OCH₃ SCH═C═CH₂ CH₃ Cl (2-) OCH₃ SCH₂CN CH₃ Cl (2-) OCH₃ SCH₂CH₂CN CH₃ Cl (2-) OCH₃ OCH₃ CH₃ Cl (2-) OCH₃ OC₂H₅ CH₃ Cl (2-) OCH₃ OC₃H₇ CH₃ Cl (2-) OCH₃ OC₃H₇-i CH₃ Cl (2-) OCH₃ OC₄H₉ CH₃ Cl (2-) OCH₃ OCH₂CF₃ CH₃ Cl (2-) OCH₃

CH₃ Cl (2-) OCH₃ OC₆H₅ CH₃ Cl (2-) OCH₃ H CH₃ Cl (2-) OCH₃ CH₃ CH₃ Cl (2-) OCH₃ C₂H₅ CH₃ Cl (2-) OCH₃ C₃H₇ CH₃ Cl (2-) OCH₃ C₃H₇-i CH₃ Cl (2-) OCH₃ C₄H₉ CH₃ Cl (2-) OCH₃ C₄H₉-i CH₃ Cl (2-) OCH₃ C₄H₉-s CH₃ Cl (2-) OCH₃ C₄H₉-t CH₃ Cl (2-) OCH₃

CH₃ Cl (2-) OCH₃

CH₃ Cl (2-) OCH₃ CH═CHCH₃ CH₃ Cl (2-) OCH₃

CH₃ Cl (2-) OCH₃

CH₃ Cl (2-) OCH₃

CH₃ Cl (2-) OCH₃ N(CH₃)₂ CH₃ Cl (2-) OCH₃

CH₃ Cl (2-) OCH₃ Cl CH₃ Cl (2-) OCH₃ Br CH₃ SO₂CH₃ (2-) OCH₃ CF₃ CH₃ SO₂CH₃ (2-) OCH₃ SCH₃ CH₃ SO₂CH₃ (2-) OCH₃ SC₂H₅ CH₃ SO₂CH₃ (2-) OCH₃ SC₃H₇ CH₃ SO₂CH₃ (2-) OCH₃ SC₃H₇-i CH₃ SO₂CH₃ (2-) OCH₃

CH₃ SO₂CH₃ (2-) OCH₃

CH₃ SO₂CH₃ (2-) OCH₃

CH₃ SO₂CH₃ (2-) OCH₃

CH₃ SO₂CH₃ (2-) OCH₃

CH₃ SO₂CH₃ (2-) OCH₃ SCH═C═CH₂ CH₃ SO₂CH₃ (2-) OCH₃ SCH₂CN CH₃ SO₂CH₃ (2-) OCH₃ SCH₂CH₂CN CH₃ SO₂CH₃ (2-) OCH₃ OCH₃ CH₃ SO₂CH₃ (2-) OCH₃ OC₂H₅ CH₃ SO₂CH₃ (2-) OCH₃ OC₃H₇ CH₃ SO₂CH₃ (2-) OCH₃ OC₃H₇-i CH₃ SO₂CH₃ (2-) OCH₃ OC₄H₉ CH₃ SO₂CH₃ (2-) OCH₃ OCH₂CF₃ CH₃ SO₂CH₃ (2-) OCH₃

CH₃ SO₂CH₃ (2-) OCH₃ OC₆H₅ CH₃ SO₂CH₃ (2-) OCH₃ H CH₃ SO₂CH₃ (2-) OCH₃ CH₃ CH₃ SO₂CH₃ (2-) OCH₃ C₂H₅ CH₃ SO₂CH₃ (2-) OCH₃ C₃H₇ CH₃ SO₂CH₃ (2-) OCH₃ C₃H₇-i CH₃ SO₂CH₃ (2-) OCH₃ C₄H₉ CH₃ SO₂CH₃ (2-) OCH₃ C₄H₉-i CH₃ SO₂CH₃ (2-) OCH₃ C₄H₉-s CH₃ SO₂CH₃ (2-) OCH₃ C₄H₉-t CH₃ SO₂CH₃ (2-) OCH₃

CH₃ SO₂CH₃ (2-) OCH₃

CH₃ SO₂CH₃ (2-) OCH₃ CH═CHCH₃ CH₃ SO₂CH₃ (2-) OCH₃

CH₃ SO₂CH₃ (2-) OCH₃

CH₃ SO₂CH₃ (2-) OCH₃

CH₃ SO₂CH₃ (2-) OCH₃ N(CH₃)₂ CH₃ SO₂CH₃ (2-) OCH₃

CH₃ SO₂CH₃ (2-) OCH₃ Cl CH₃ SO₂CH₃ (2-) OCH₃ Br CH₃ Cl (2-) OCH₃ CF₃

Cl (2-) OCH₃ SCH₃

Cl (2-) OCH₃ SC₂H₅

Cl (2-) OCH₃ SC₃H₇

Cl (2-) OCH₃ SC₃H₇-i

Cl (2-) OCH₃

Cl (2-) OCH₃

Cl (2-) OCH₃

Cl (2-) OCH₃

Cl (2-) OCH₃

Cl (2-) OCH₃ SCH═C═CH₂

Cl (2-) OCH₃ SCH₂CN

Cl (2-) OCH₃ SCH₂CH₂CN

Cl (2-) OCH₃ OCH₃

Cl (2-) OCH₃ OC₂H₅

Cl (2-) OCH₃ OC₃H₇

Cl (2-) OCH₃ OC₃H₇-i

Cl (2-) OCH₃ OC₄H₉

Cl (2-) OCH₃ OCH₂CF₃

Cl (2-) OCH₃

Cl (2-) OCH₃ OC₆H₅

Cl (2-) OCH₃ H

Cl (2-) OCH₃ CH₃

Cl (2-) OCH₃ C₂H₅

Cl (2-) OCH₃ C₃H₇

Cl (2-) OCH₃ C₃H₇-i

Cl (2-) OCH₃ C₄H₉

Cl (2-) OCH₃ C₄H₉-i

Cl (2-) OCH₃ C₄H₉-s

Cl (2-) OCH₃ C₄H₉-t

Cl (2-) OCH₃

Cl (2-) OCH₃

Cl (2-) OCH₃ CH═CHCH₃

Cl (2-) OCH₃

Cl (2-) OCH₃

Cl (2-) OCH₃

Cl (2-) OCH₃ N(CH₃)₂

Cl (2-) OCH₃

Cl (2-) OCH₃ Cl

Cl (2-) OCH₃ Br

SO₂CH₃ (2-) OCH₃ CF₃

SO₂CH₃ (2-) OCH₃ SCH₃

SO₂CH₃ (2-) OCH₃ SC₂H₅

SO₂CH₃ (2-) OCH₃ SC₃H₇

SO₂CH₃ (2-) OCH₃ SC₃H₇-i

SO₂CH₃ (2-) OCH₃

SO₂CH₃ (2-) OCH₃

SO₂CH₃ (2-) OCH₃

SO₂CH₃ (2-) OCH₃

SO₂CH₃ (2-) OCH₃

SO₂CH₃ (2-) OCH₃ SCH═C═CH₂

SO₂CH₃ (2-) OCH₃ SCH₂CN

SO₂CH₃ (2-) OCH₃ SCH₂CH₂CN

SO₂CH₃ (2-) OCH₃ OCH₃

SO₂CH₃ (2-) OCH₃ OC₂H₅

SO₂CH₃ (2-) OCH₃ OC₃H₇

SO₂CH₃ (2-) OCH₃ OC₃H₇-i

SO₂CH₃ (2-) OCH₃ OC₄H₉

SO₂CH₃ (2-) OCH₃ OCH₂CF₃

SO₂CH₃ (2-) OCH₃

SO₂CH₃ (2-) OCH₃ OC₆H₅

SO₂CH₃ (2-) OCH₃ H

SO₂CH₃ (2-) OCH₃ CH₃

SO₂CH₃ (2-) OCH₃ C₂H₅

SO₂CH₃ (2-) OCH₃ C₃H₇

SO₂CH₃ (2-) OCH₃ C₃H₇-i

SO₂CH₃ (2-) OCH₃ C₄H₉

SO₂CH₃ (2-) OCH₃ C₄H₉-i

SO₂CH₃ (2-) OCH₃ C₄H₉-s

SO₂CH₃ (2-) OCH₃ C₄H₉-t

SO₂CH₃ (2-) OCH₃

SO₂CH₃ (2-) OCH₃

SO₂CH₃ (2-) OCH₃ CH═CHCH₃

SO₂CH₃ (2-) OCH₃

SO₂CH₃ (2-) OCH₃

SO₂CH₃ (2-) OCH₃

SO₂CH₃ (2-) OCH₃ N(CH₃)₂

SO₂CH₃ (2-) OCH₃

SO₂CH₃ (2-) OCH₃ Cl

SO₂CH₃ (2-) OCH₃ Br

Cl (2-) OCH₃ CF₃ N(CH₃)₂ Cl (2-) OCH₃ SCH₃ N(CH₃)₂ Cl (2-) OCH₃ SC₂H₅ N(CH₃)₂ Cl (2-) OCH₃ SC₃H₇ N(CH₃)₂ Cl (2-) OCH₃ SC₃H₇-i N(CH₃)₂ Cl (2-) OCH₃

N(CH₃)₂ Cl (2-) OCH₃

N(CH₃)₂ Cl (2-) OCH₃

N(CH₃)₂ Cl (2-) OCH₃

N(CH₃)₂ Cl (2-) OCH₃

N(CH₃)₂ Cl (2-) OCH₃ SCH═C═CH₂ N(CH₃)₂ Cl (2-) OCH₃ SCH₂CN N(CH₃)₂ Cl (2-) OCH₃ SCH₂CH₂CN N(CH₃)₂ Cl (2-) OCH₃ OCH₃ N(CH₃)₂ Cl (2-) OCH₃ OC₂H₅ N(CH₃)₂ Cl (2-) OCH₃ OC₃H₇ N(CH₃)₂ Cl (2-) OCH₃ OC₃H₇-i N(CH₃)₂ Cl (2-) OCH₃ OC₄H₉ N(CH₃)₂ Cl (2-) OCH₃ OCH₂CF₃ N(CH₃)₂ Cl (2-) OCH₃

N(CH₃)₂ Cl (2-) OCH₃ OC₆H₅ N(CH₃)₂ Cl (2-) OCH₃ H N(CH₃)₂ Cl (2-) OCH₃ CH₃ N(CH₃)₂ Cl (2-) OCH₃ C₂H₅ N(CH₃)₂ Cl (2-) OCH₃ C₃H₇ N(CH₃)₂ Cl (2-) OCH₃ C₃H₇-i N(CH₃)₂ Cl (2-) OCH₃ C₄H₉ N(CH₃)₂ Cl (2-) OCH₃ C₄H₉-i N(CH₃)₂ Cl (2-) OCH₃ C₄H₉-s N(CH₃)₂ Cl (2-) OCH₃ C₄H₉-t N(CH₃)₂ Cl (2-) OCH₃

N(CH₃)₂ Cl (2-) OCH₃

N(CH₃)₂ Cl (2-) OCH₃ CH═CHCH₃ N(CH₃)₂ Cl (2-) OCH₃

N(CH₃)₂ Cl (2-) OCH₃

N(CH₃)₂ Cl (2-) OCH₃

N(CH₃)₂ Cl (2-) OCH₃ N(CH₃)₂ N(CH₃)₂ Cl (2-) OCH₃

N(CH₃)₂ Cl (2-) OCH₃ Cl N(CH₃)₂ Cl (2-) OCH₃ Br N(CH₃)₂ SO₂CH₃ (2-) OCH₃ CF₃ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ SCH₃ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ SC₂H₅ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ SC₃H₇ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ SC₃H₇-i N(CH₃)₂ SO₂CH₃ (2-) OCH₃

N(CH₃)₂ SO₂CH₃ (2-) OCH₃

N(CH₃)₂ SO₂CH₃ (2-) OCH₃

N(CH₃)₂ SO₂CH₃ (2-) OCH₃

N(CH₃)₂ SO₂CH₃ (2-) OCH₃

N(CH₃)₂ SO₂CH₃ (2-) OCH₃ SCH═C═CH₂ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ SCH₂CN N(CH₃)₂ SO₂CH₃ (2-) OCH₃ SCH₂CH₂CN N(CH₃)₂ SO₂CH₃ (2-) OCH₃ OCH₃ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ OC₂H₅ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ OC₃H₇ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ OC₃H₇-i N(CH₃)₂ SO₂CH₃ (2-) OCH₃ OC₄H₉ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ OCH₂CF₃ N(CH₃)₂ SO₂CH₃ (2-) OCH₃

N(CH₃)₂ SO₂CH₃ (2-) OCH₃ OC₆H₅ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ H N(CH₃)₂ SO₂CH₃ (2-) OCH₃ CH₃ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ C₂H₅ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ C₃H₇ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ C₃H₇-i N(CH₃)₂ SO₂CH₃ (2-) OCH₃ C₄H₉ N(CH₃)₂ SO₂CH₃ (2-) OCH₃ C₄H₉-i N(CH₃)₂ SO₂CH₃ (2-) OCH₃ C₄H₉-s N(CH₃)₂ SO₂CH₃ (2-) OCH₃ C₄H₉-t N(CH₃)₂ SO₂CH₃ (2-) OCH₃

N(CH₃)₂ SO₂CH₃ (2-) OCH₃

N(CH₃)₂ SO₂CH₃ (2-) OCH₃ CH═CHCH₃ N(CH₃)₂ SO₂CH₃ (2-) OCH₃

N(CH₃)₂ SO₂CH₃ (2-) OCH₃

N(CH₃)₂ SO₂CH₃ (2-) OCH₃

N(CH₃)₂ SO₂CH₃ (2-) OCH₃ N(CH₃)₂ N(CH₃)₂ SO₂CH₃ (2-) OCH₃

N(CH₃)₂ SO₂CH₃ (2-) OCH₃ Cl N(CH₃)₂ SO₂CH₃ (2-) OCH₃ Br N(CH₃)₂ Cl (2-) OCH₃ CH₃ OCH₃ Cl (2-) OCH₃ C₂H₅ OCH₃ Cl (2-) OCH₃ C₃H₇ OCH₃ Cl (2-) OCH₃ SCH₃ OCH₃ Cl (2-) OCH₃ SC₂H₅ OCH₃ Cl (2-) OCH₃ OCH₃ OCH₃ Cl (2-) OCH₃ OC₂H₅ OCH₃ Cl (2-) OCH₃ CH₃ OC₂H₅ Cl (2-) OCH₃ C₂H₅ OC₂H₅ Cl (2-) OCH₃ C₃H₇ OC₂H₅ Cl (2-) OCH₃ SCH₃ OC₂H₅ Cl (2-) OCH₃ SC₂H₅ OC₂H₅ Cl (2-) OCH₃ OCH₃ OC₂H₅ Cl (2-) OCH₃ OC₂H₅ OC₂H₅ SO₂CH₃ (2-) OCH₃ Cl OCH₃ SO₂CH₃ (2-) OCH₃ Br OCH₃ SO₂CH₃ (2-) OCH₃ CH₃ OCH₃ SO₂CH₃ (2-) OCH₃ C₂H₅ OCH₃ SO₂CH₃ (2-) OCH₃ C₃H₇ OCH₃ SO₂CH₃ (2-) OCH₃ SCH₃ OCH₃ SO₂CH₃ (2-) OCH₃ SC₂H₅ OCH₃ SO₂CH₃ (2-) OCH₃ OCH₃ OC₂H₅ SO₂CH₃ (2-) OCH₃ OC₂H₅ OC₂H₅ SO₂CH₃ (2-) OCH₃ CH₃ OC₂H₅ SO₂CH₃ (2-) OCH₃ C₂H₅ OC₂H₅ SO₂CH₃ (2-) OCH₃ C₃H₇ OC₂H₅ SO₂CH₃ (2-) OCH₃ SCH₃ OC₂H₅ SO₂CH₃ (2-) OCH₃ SC₂H₅ OC₂H₅ SO₂CH₃ (2-) OCH₃ OCH₃ OC₂H₅ Cl (2-) F OCH₃ CH₃ Cl (2-) F OCH₃ C₂H₅ Cl (2-) F C₂H₅ OCH₃ Cl (2-) F C₂H₅ C₂H₅ Cl (2-) F OC₂H₅ CH₃ Cl (2-) F OC₂H₅ C₂H₅ Cl (2-) F OCH₃

Cl (2-) F OC₂H₅

Cl (2-) F SCH₃ CH₃ Cl (2-) F SCH₃

Cl (2-) F CH₃ CH₃ Cl (2-) F CH₃

[0085] Group 7

[0086] Here, R³, R⁴, R⁵ and R⁶ each have, for example, the meanings given above in Group 6.

[0087] Group 8

[0088] Here, R³, R⁴, R⁵ and R⁶ each have, for example, the meanings given above in Group 6.

[0089] Group 9

[0090] Here, R³, R⁴, R⁵ and R⁶ each have, for example, the meanings given above in Group 6.

[0091] Group 10

[0092] Here, R³, R⁴, R and R⁶ each have, for example, the meanings given above in Group 6.

[0093] The novel substituted benzoylcyclohexenones of the formula (I) have strong and selective herbicidal activity.

[0094] The novel substituted benzoylcyclohexenones of the formula (I) are obtained when substituted cyclohexanediones of the formula (II)

[0095] in which

[0096] A, R¹, R², R³, R⁴ and Z are as defined above,

[0097] are reacted with a halogenating agent, if appropriate in the presence of a reaction auxiliary and if appropriate in the presence of a diluent, and the halogenocyclohexenones obtained in this way (in the first reaction step), of the formula (III)

[0098] in which

[0099] A, R¹, R², R³, R⁴ and Z are as defined above,

[0100] X represents halogen, preferably represents fluorine or chlorine, particularly preferably represents chlorine,

[0101] after intermediate isolation or without intermediate isolation (“in situ”)

[0102] are reacted in a second reaction step with mercapto compounds of the formula (IV)

HS—Y  (IV)

[0103] in which

[0104] Y is as defined above,

[0105] if appropriate in the presence of a reaction auxiliary and if appropriate in the presence of a diluent,

[0106] and, if appropriate, the compounds of the formula (I) obtained in this manner are subsequently subjected in a customary manner, within the scope of the definition of the substituents, to electrophilic or nucleophilic substitution reactions or oxidation or reduction reactions, or the compounds of the formula (I) are converted in a customary manner into salts.

[0107] Using, for example 2-[4-chloro-2-[(3,4-dimethyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl)-methyl]-benzoyl]-cyclohexane-1,3-dione and phosgene and then thiophenol as starting materials, the course of the reaction in the process according to the invention can be illustrated by the following equation

[0108] The formula (II) provides a general definition of the substituted benzoylcyclohexanediones to be used as starting materials in the process according to the invention for preparing compounds of the general formula (I). In the general formula (II), A, R¹, R², R³, R⁴ and Z each preferably have those meanings which have already been mentioned above, in connection with the description of the compounds of the general formula (I) according to the invention, as being preferred, particularly preferred, very particularly preferred or most preferred for A, R¹, R², R³, R⁴ and Z.

[0109] The starting materials of the general formula (II) are known and/or can be prepared by processes known per se (cf. WO-A-00/05221).

[0110] The first reaction step of the process according to the invention for preparing the compounds of the general of the general formula (I) is carried out using a halogenating agent. The halogenating agent used can be a customary halogenating agent suitable for converting enols into the corresponding halogenoalkenes. Here, halogen preferably represents fluorine, chlorine or bromine, in particular chlorine, i.e. preference is given to using chlorinating agents or brominating agents. These include, preferably, phosgene, oxalyl chloride, oxalyl bromide, phosphorus(III) chloride, phosphorus(III) bromide, phosphoryl chloride, thionyl chloride and thionyl bromide.

[0111] The first reaction step of the process according to the invention for preparing the compounds of the general formula (I) is preferably carried out using a reaction auxiliary. Suitable reaction auxiliaries are the reaction auxiliaries customarily used for halogenating reactions. These preferably include acetonitrile, N,N-dimethylformamide, N,N-diethyl-formamide, N,N-dipropyl-formamide and N,N-dibutylformamide, and also N-methyl-pyrrolidone.

[0112] The formula (IV) provides a general definition of the mercapto compounds further to be used as starting materials in the process according to the invention for preparing compounds of the general formula (I). In the general formula (IV), Y preferably has in particular that meaning which has already been mentioned above, in connection with the description of the compounds of the general formula (I) according to the invention, as being preferred, particularly preferred or very particularly preferred for Y.

[0113] The starting materials of the general formula (IV) are known organic chemicals for synthesis.

[0114] The second reaction step of the process according to the invention for preparing compounds of the general formula (I) is preferably carried out using a reaction auxiliary. Suitable reaction auxiliaries are, in general, the customary inorganic or organic bases or acid acceptors. These preferably include alkali metal or alkaline earth metal acetates, amides, carbonates, bicarbonates, hydrides, hydroxides or alkoxides, such as, for example, sodium acetate, potassium acetate or calcium acetate, lithium amide, sodium amide, potassium amide or calcium amide, sodium carbonate, potassium carbonate or calcium carbonate, sodium bicarbonate, potassium bicarbonate or calcium bicarbonate, lithium hydride, sodium hydride, potassium hydride or calcium hydride, lithium hydroxide, sodium hydroxide, potassium hydroxide or calcium hydroxide, sodium methoxide, ethoxide, n- or i-propoxide, n-, i-, s- or t-butoxide or potassium methoxide, ethoxide, n- or i-propoxide, n-, i-, s- or t-butoxide; furthermore also basic organic nitrogen compounds, such as, for example, trimethylamine, triethylamine, tripropylamine, tributylamine, ethyl-diisopropylamine, N,N-dimethyl-cyclohexylamine, dicyclohexylamine, ethyl-dicyclohexylamine, N,N-dimethyl-aniline, N,N-dimethyl-benzylamine, pyridine, 2-methyl-, 3-methyl-, 4-methyl-, 2,4-dimethyl-, 2,6-dimethyl-, 3,4-dimethyl- and 3,5-dimethylpyridine, 5-ethyl-2-methyl-pyridine, 4-dimethylamino-pyridine, N-methyl-piperidine, 1,4-diazabicyclo[2.2.2]-octane (DABCO), 1,5-diazabicyclo[4.3.0]-non-5-ene (DBN), or 1,8 diazabicyclo[5.4.0]-undec-7-ene (DBU).

[0115] The first and the second step of the process according to the invention for preparing the compounds of the general formula (I) are preferably carried out using diluents. Suitable diluents are especially inert organic solvents. These include, in particular, aliphatic, alicyclic or aromatic, optionally halogenated hydrocarbons, such as, for example, benzine, benzene, toluene, xylene, chlorobenzene, dichlorobenzene, petroleum ether, hexane, cyclohexane, dichloromethane, chloroform, carbon tetrachloride; ethers, such as diethyl ether, diisopropyl ether, dioxane, tetrahydrofuran or ethylene glycol dimethyl ether or ethylene glycol diethyl ether; ketones, such as acetone, butanone or methyl isobutyl ketone; nitriles, such as acetonitrile, propionitrile or butyronitrile; amides, such as N,N-dimethylformamide, N,N-dimethylacetamide, N-methyl-formanilide, N-methyl-pyrrolidone or hexamethylphosphoric triamide; esters, such as methyl acetate or ethyl acetate; sulphoxides, such as dimethyl sulphoxide; alcohols, such as methanol, ethanol, n- or i-propanol, ethylene glycol monomethyl ether or ethylene glycol monoethyl ether.

[0116] When carrying out the first and the second step of the process according to the invention, the reaction temperatures can be varied within a relatively wide range. In general, the steps are carried out at temperatures between −20° C. and +150° C., preferably between 0° C. and 120° C.

[0117] The two steps of the process according to the invention are generally carried out under atmospheric pressure. However, it is also possible to carry out the process according to the invention under elevated or reduced pressure—in general between 0.1 bar and 10 bar.

[0118] For carrying out the process according to the invention, the starting materials are generally employed in approximately equimolar amounts. However, it is also possible to use a relatively large excess of one of the components. The reaction is generally carried out in a suitable diluent in the presence of a suitable reaction auxiliary and the reaction mixture is generally stirred at the required temperature for several hours. Work-up is carried out by customary methods (cf. the Preparation Examples).

[0119] The active compounds according to the invention can be used as defoliants, desiccants, haulm killers and, especially, as weed killers. Weeds in the broadest sense are understood to mean all plants which grow in locations where they are undesired. Whether the substances according to the invention act as total or selective herbicides depends essentially on the amount used.

[0120] The active compounds according to the invention can be used, for example, in connection with the following plants:

[0121] Dicotyledonous weeds of the genera: Abutilon, Amaranthus, Ambrosia, Anoda, Anthemis, Aphanes, Atriplex, Bellis, Bidens, Capsella, Carduus, Cassia, Centaurea, Chenopodium, Cirsium, Convolvulus, Datura, Desmodium, Emex, Erysimum, Euphorbia, Galeopsis, Galinsoga, Galium, Hibiscus, Ipomoea, Kochia, Lamium, Lepidium, Lindemia, Matricaria, Mentha, Mercurialis, Mullugo, Myosotis, Papaver, Pharbitis, Plantago, Polygonum, Portulaca, Ranunculus, Raphanus, Rorippa, Rotala, Rumex, Salsola, Senecio, Sesbania, Sida, Sinapis, Solanum, Sonchus, Sphenoclea, Stellaria, Taraxacum, Thlaspi, Trifolium, Urtica, Veronica, Viola, Xanthium.

[0122] Dicotyledonous crops of the genera: Arachis, Beta, Brassica, Cucumis, Cucurbita, Helianthus, Daucus, Glycine, Gossypium, Ipomoea, Lactuca, Linum, Lycopersicon, Nicotiana, Phaseolus, Pisum, Solanum, Vicia.

[0123] Monocotyledonous weeds of the genera: Aegilops, Agropyron, Agrostis, Alopecurus, Apera, Avena, Brachiaria, Bromus, Cenchrus, Commelina, Cynodon, Cyperus, Dactyloctenium, Digitaria, Echinochloa, Eleocharis, Eleusine, Eragrostis, Eriochloa, Festuca, Fimbristylis, Heteranthera, Imperata, Ischaemum, Leptochloa, Lolium, Monochoria, Panicum, Paspalum, Phalaris, Phleum, Poa, Rottboellia, Sagittaria, Scirpus, Setaria, Sorghum.

[0124] Monocotyledonous crops of the genera: Allium, Ananas, Asparagus, Avena, Hordeum, Oryza, Panicum, Saecharum, Secale, Sorghum, Triticale, Triticum, Zea.

[0125] However, the use of the active compounds according to the invention is in no way restricted to these genera, but also extends in the same manner to other plants.

[0126] The active compounds according to the invention are suitable, depending on the concentration, for the total control of weeds, for example on industrial terrain and rail tracks, and on paths and areas with and without tree plantings. Similarly, the active compounds according to the invention can be employed for controlling weeds in perennial crops, for example forests, decorative tree plantings, orchards, vineyards, citrus groves, nut orchards, banana plantations, coffee plantations, tea plantations, rubber plantations, oil palm plantations, cocoa plantations, soft fruit plantings and hop fields, on lawns, turf and pastureland, and for the selective control of weeds in annual crops.

[0127] The compounds of the formula (I) according to the invention have strong herbicidal activity and a broad activity spectrum when used on the soil or on above-ground parts of plants. To a certain extent, they are also suitable for the selective control of monocotyledonous and dicotyledonous weeds in monocotyledonous and dicotyledonous crops, both by the pre-emergence and by the post-emergence method.

[0128] At certain concentrations or application rates, the active compounds according to the invention can also be employed for controlling animal pests and fungal or bacterial plant diseases. If appropriate, they can also be used as intermediates or precursors for the synthesis of other active compounds.

[0129] According to the invention, it is possible to treat all plants and parts of plants. Plants are to be understood here as meaning all plants and plant populations such as desired and undesired wild plants or crop plants (including naturally occurring crop plants). Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including plant cultivars which can or cannot be protected by plant breeders' certificates. Parts of plants are to be understood as meaning all above-ground and below-ground parts and organs of plants, such as shoot, leaf, flower and root, examples which may be mentioned being leaves, needles, stems, trunks, flowers, fruit-bodies, fruits and seeds and also roots, tubers and rhizomes. Parts of plants also include harvested plants and vegetative and generative propagation material, for example seedlings, tubers, rhizomes, cuttings and seeds.

[0130] The treatment of the plants and parts of plants according to the invention with the active compounds is carried out directly or by action on their environment, habitat or storage area according to customary treatment methods, for example by dipping, spraying, evaporating, atomizing, broadcasting, brushing-on and, in the case of propagation material, in particular in the case of seeds, furthermore by one- or multi-layer coating.

[0131] The active compounds can be converted into the customary formulations, such as solutions, emulsions, wettable powders, suspensions, powders, dusts, pastes, soluble powders, granules, suspo-emulsion concentrates, natural and synthetic substances impregnated with active compound, and microencapsulations in polymeric substances.

[0132] These formulations are produced in a known manner, for example by mixing the active compounds with extenders, that is to say liquid solvents and/or solid carriers, optionally with the use of surfactants, that is to say emulsifiers and/or dispersants and/or foam formers.

[0133] If the extender used is water, it is also possible to use, for example, organic solvents as auxiliary solvents. Liquid solvents which are mainly suitable are: aromatics, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, alcohols, such as butanol or glycol, and also their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents, such as dimethylformamide and dimethyl sulphoxide, and water.

[0134] Suitable solid carriers are: for example ammonium salts and ground natural minerals, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as finely divided silica, alumina and silicates; suitable solid carriers for granules are: for example crushed and fractionated natural rocks, such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules of inorganic and organic meals, and granules of organic material, such as sawdust, coconut shells, maize cobs and tobacco stalks; suitable emulsifiers and/or foam formers are: for example nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates, arylsulphonates and protein hydrolysates; suitable dispersants are: for example lignosulphite waste liquors and methylcellulose.

[0135] Tackifiers, such as carboxymethylcellulose, natural and synthetic polymers in the form of powders, granules or latices, such as gum arabic, polyvinyl alcohol and polyvinyl acetate, and also natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids can be used in the formulations. Other possible additives are mineral and vegetable oils.

[0136] It is possible to use colorants, such as inorganic pigments, for example iron oxide, titanium oxide, Prussian blue, and organic dyestuffs, such as alizarin dyestuffs, azo dyestuffs and metal phthalocyanine dyestuffs, and trace nutrients, such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.

[0137] The formulations generally comprise between 0.1 and 95 percent by weight of active compound, preferably between 0.5 and 90%.

[0138] For controlling weeds, the active compounds according to the invention, as such or in their formulations, can also be used as mixtures with known herbicides and/or substances which improve the compatibility with crop plants (“safeners”), finished formulations or tank mixes being possible. Also possible are mixtures with weed-killers comprising one or more known herbicides and a safener.

[0139] Possible components for the mixtures are known herbicides, for example

[0140] acetochlor, acifluorfen (-sodium), aclonifen, alachlor, alloxydim (-sodium), ametryne, amicarbazone, amidochlor, amidosulfuron, anilofos, asulam, atrazine, azafenidin, azimsulfuron, beflubutamid, benazolin (-ethyl), benfuresate, bensulfuron (-methyl), bentazon, benzfendizone, benzobicyclon, benzofenap, benzoylprop (-ethyl), bialaphos, bifenox, bispyribac (-sodium), bromobutide, bromofenoxim, bromoxynil, butachlor, butafenacil (-allyl), butroxydim, butylate, cafenstrole, caloxydim, carbetamide, carfentrazone (-ethyl), chlomethoxyfen, chloramben, chloridazon, chlorimuron (-ethyl), chlomitrofen, chlorsulfuron, chlortoluron, cinidon (-ethyl), cinmethylin, cinosulfuron, clefoxydim, clethodim, clodinafop (-propargyl), clomazone, clomeprop, clopyralid, clopyrasulfuron (-methyl), cloransulam (-methyl), cumyluron, cyanazine, cybutryne, cycloate, cyclosulfamuron, cycloxydim, cyhalofop (-butyl), 2,4-D, 2,4-DB, desmedipham, diallate, dicamba, dichlorprop (-P), diclofop (-methyl), diclosulam, diethatyl (-ethyl), difenzoquat, diflufenican, diflufenzopyr, dimefuron, dimepiperate, dimethachlor, dimethametryn, dimethenamid, dimexyflam, dinitramine, diphenamid, diquat, dithiopyr, diuron, dymron, epropodan, EPTC, esprocarb, ethalfluralin, ethametsulfuron (-methyl), ethofumesate, ethoxyfen, ethoxysulfuron, etobenzanid, fenoxaprop (-P-ethyl), fentrazamide, flamprop (-isopropyl, -isopropyl-L, -methyl), flazasulfuron, florasulam, fluazifop (-P-butyl), fluazolate, flucarbazone (-sodium), flufenacet, flumetsulam, flumiclorac (-pentyl), flumioxazin, flumipropyn, flumetsulam, fluometuron, fluorochloridone, fluoroglycofen (-ethyl), flupoxam, flupropacil, flurpyrsulfuron (-methyl, -sodium), flurenol (-butyl), fluridone, fluroxypyr (-butoxypropyl, -meptyl), flurprimidol, flurtamone, fluthiacet (-methyl), fluthiamide, fomesafen, foramsulfuron, glufosinate (-ammonium), glyphosate (-isopropylammonium), halosafen, haloxyfop (-ethoxyethyl, -P-methyl), hexazinone, imazamethabenz (-methyl), imazamethapyr, imazamox, imazapic, imazapyr, imazaquin, imazethapyr, imazosulfuron, iodosulfuron (-methyl, -sodium), ioxynil, isopropalin, isoproturon, isouron, isoxaben, isoxachlortole, isoxaflutole, isoxapyrifop, lactofen, lenacil, linuron, MCPA, mecoprop, mefenacet, mesotrione, metamitron, metazachlor, methabenzthiazuron, metobenzuron, metobromuron, (alpha-)metolachlor, metosulam, metoxuron, metribuzin, metsulfuron (-methyl), molinate, monolinuron, naproanilide, napropamide, neburon, nicosulfuron, norflurazon, orbencarb, oryzalin, oxadiargyl, oxadiazon, oxasulfuron, oxaziclomefone, oxyfluorfen, paraquat, pelargonic acid, pendimethalin, pendralin, pentoxazone, phemnedipham, picolinafen, piperophos, pretilachlor, primisulfuron (-methyl), profluazol, prometryn, propachlor, propanil, propaquizafop, propisochlor, procarbazone (-sodium), propyzamide, prosulfocarb, prosulfuron, pyraflufen (-ethyl), pyrazogyl, pyrazolate, pyrazosulfuron (-ethyl), pyrazoxyfen, pyribenzoxim, pyributicarb, pyridate, pyridatol, pyriftalid, pyriminobac (-methyl), pyrithiobac (-sodium), quinchlorac, quinmerac, quinoclamine, quizalofop (-P-ethyl, -P-tefuryl), rimsulfuron, sethoxydim, simazine, simetryn, sulcotrione, sulfentrazone, sulfometuron (-methyl), sulfosate, sulfosulfuron, tebutam, tebuthiuron, tepraloxydim, terbuthylazine, terbutryn, thenylchlor, thiafluamide, thiazopyr, thidiazimin, thifensulfuron (-methyl), thiobencarb, tiocarbazil, tralkoxydim, triallate, triasulfuron, tribenuron (-methyl), triclopyr, tridiphane, trifluralin, trifloxysulfuron, triflusulfuron (-methyl), tritosulfuron.

[0141] A mixture with other known active compounds, such as fungicides, insecticides, acaricides, nematicides, bird repellents, plant nutrients and agents which improve soil structure, is also possible.

[0142] The active compounds can be used as such, in the form of their formulations or in the use forms, prepared therefrom by further dilution, such as ready-to-use solutions, suspensions, emulsions, powders, pastes and granules. They are used in a customary manner, for example by watering, spraying, atomizing or broadcasting.

[0143] The active compounds according to the invention can be applied both before and after emergence of the plants. They can also be incorporated into the soil before sowing.

[0144] The amount of active compound used can vary within a relatively wide range. It depends essentially on the nature of the desired effect. In general, the amounts used are between 1 g and 10 kg of active compound per hectare of soil surface, preferably between 5 g and 5 kg per ha.

[0145] The preparation and the use of the active compounds according to the invention is illustrated by the examples below.

PREPARATION EXAMPLES Example 1

[0146]

[0147] A mixture of 1.3 g (3 mmol) of 2-[2,4-dichloro-3-[(3-methyl-2-oxo-tetrahydro-1(2H)-pyrimidinyl)-methyl]-benzoyl]-cyclohexane-1,3-dione, 1.0 g (7.5 mmol) of oxalyl chloride, 2 drops of N,N-dimethyl-formamide and 30 ml of methylene chloride is heated under reflux for 30 minutes and then concentrated under water pump vacuum. The residue is taken up in 50 ml of tetrahydrofuran and admixed with 0.33 g (3 mmol) of thiophenol. With ice-cooling, 0.50 g (4.5 mmol) of triethylamine is then added dropwise. The ice-cooling is removed, and the mixture is then stirred at room temperature for 2 hours and subsequently concentrated under water pump vacuum. The residue is taken up in methylene chloride, washed once each with 1N hydrochloric acid, water and saturated aqueous sodium chloride solution, dried with sodium sulphate and filtered. The filtrate is concentrated under water pump vacuum, the residue is digested with diethyl ether and the resulting crystalline product is isolated by filtration with suction.

[0148] This gives 0.91 g (61% of theory) of 1-[2,6-dichloro-3-[(6-oxo-2-phenylthio-1-cyclohexen-1-yl)-carbonyl]-benzyl]-3-methyl-tetrahydro-2(1H)-pyrimidinone of melting point 140° C.

[0149] Analogously to Example 1 and in accordance with the general description of the preparation process according to the invention, it is also possible to prepare, for example, the compounds of the general formula (I)—or those of the general formula (ID)—listed in Table 1 below. TABLE 1 Examples of compounds of the formula (ID) (ID)

Ex. (position) (position) (position) Physical No. n R³ R⁴ —A-Z Y data 2 0 (2) (4) (3) C₆H₅ m.p.: 169° C. Cl Cl

logP = 3.02^(a)) 3 0 (2) (4) (3) C₆H₅ m.p.: 149° C. Cl Cl

logP = 3.30^(a)) 4 0 (2) (4) (3) C₆H₅ m.p.: 159° C. Cl Cl

logP = 3.29^(a)) 5 0 (2) (4) (3) C₆H₅ m.p.: 163° C. Cl Cl

logP = 3.50^(a)) 6 0 (2) (4) (3) C₆H₅ m.p.: 195° C. Cl SO₂CH₃

logP = 2.84^(a)) 7 0 (2) (4) (3) C₆H₅ m.p.: 234° C. Cl SO₂CH₃

logP = 2.67^(a)) 8 0 (2) (4) (3) C₆H₅ m.p.: 203° C. Cl SO₂CH₃

logP = 2.56^(a)) 9 0 (2) (4) (3) C₆H₅ m.p.: 184° C. Cl SO₂CH₃

logP = 2.79^(a)) 10 0 (2) (4) (3) C₆H₅ m.p.: 228° C. Cl SO₂CH₃

logP = 3.13^(a)) 11 0 (2) (4) (3) C₆H₅ m.p.: 176° C. Cl Cl

logP = 3.06^(a)) 12 0 (2) (4) (3) C₆H₅ m.p.: 145° C. Cl Cl

logP = 3.69^(a)) 13 0 (2) (4) (3) C₆H₅ m.p.: 207° C. Cl Cl

logP = 3.10^(a)) 14 2 (2) (4) (3) C₆H₅ m.p.: 180° C. Cl Cl

logP = 2.62^(a)) 15 1 (2) (4) (3) C₆H₅ Cl Cl

16 0 (4) — (2) C₆H₅ logP = 3.58^(a)) CF₃

17 0 (4) — (2) CH₃ logP = 2.63^(a)) CF₃

18 0 (4) — (2) C₆H₅ logP = 3.30^(a)) CF₃

19 0 (4) — (2) CH₃ logP = 2.41^(a)) CF₃

20 0 (4) — (2) C₆H₅ logP = 3.25^(a)) CF₃

21 0 (2) (4) (3) C₆H₅ Cl Cl

22 0 (2) (4) (3) C₆H₅ Cl SO₂CH₃

23 0 (2) (4) (3) C₆H₅ Cl SO₂CH₃

24 0 (2) (4) (3) C₆H₅ Cl Cl

25 0 (2) (4) (3) C₆H₅ Cl Cl

26 0 (2) (4) (3) C₆H₅ Cl SO₂CH₃

27 0 (2) (4) (3) C₆H₅ Cl Cl

28 0 (2) (4) (3) C₆H₅ Cl Cl

29 0 (2) (4) (3) C₆H₅ Cl Cl

30 0 (2) (4) (3) C₆H₅ Cl Cl

31 0 (2) (4) (3) C₆H₅ Cl Cl

32 0 (2) (4) (3) C₆H₅ Cl Cl

33 0 (2) (4) (3) C₆H₅ Cl Cl

34 0 (2) (4) (3) C₆H₅ Cl Cl

35 0 (2) (4) (3) C₆H₅ Cl Cl

36 0 (2) (4) (3) C₆H₅ Cl Cl

37 0 (2) (4) (3) C₆H₅ Cl Cl

38 0 (2) (4) (3) C₆H₅ Cl Cl

39 0 (2) (4) (3) C₆H₅ Cl SO₂CH₃

40 0 (2) (4) (3) C₆H₅ Cl SO₂CH₃

41 0 (2) (4) (3) C₆H₅ Cl SO₂CH₃

42 0 (2) (4) (3) C₆H₅ OCH₃ Cl

43 0 (2) (4) (3) C₆H₅ OCH₃ Cl

44 0 (2) (4) (3) C₆H₅ OCH₃ Cl

45 0 (2) (4) (3) C₆H₅ OCH₃ Cl

46 0 (2) (4) (3) C₆H₅ OCH₃ Cl

47 0 (2) (4) (3) C₆H₅ Cl CF₃

48 0 (2) (4) (3) C₆H₅ Cl CF₃

49 0 (2) (4) (3) C₆H₅ Cl CF₃

50 0 (2) (4) (3) C₆H₅ Cl CF₃

51 0 (2) (4) (3) C₆H₅ Cl CF₃

52 0 (2) — (4) C₆H₅ Cl

53 0 (2) (4) (3) C₆H₅ OCH₃ Cl

54 0 (2) (4) (3) C₆H₅ OCH₃ Cl

55 0 (2) (4) (3) C₆H₅ OCH₃ Cl

56 0 (2) (4) (3) C₆H₅ m.p.: 85° C. Cl SO₂CH₃

57 0 (2) (4) (3) C₆H₅ m.p.: 226° C. Cl SO₂CH₃

58 0 (2) — (4) C₆H₅ m.p.: 183° C. Cl

59 0 (2) (4) (3) C₆H₅ m.p.: 159° C. Cl SO₂CH₃

60 0 (2) — (4) C₆H₅ m.p.: 77° C. NO₂

61 0 (4) — (2) C₆H₅ m.p.: 167° C. CF₃

62 0 (2) (4) (3) C₂H₅ n_(D) ²⁰ = 1.6122 Cl Cl

63 0 (2) (4) (3) CH₃ n_(D) ²⁰ = 1.6018 Cl Cl

64 0 (2) (4) (3) C₆H₅ m.p.: 116° C. Cl SO₂CH₃

65 0 (2) — (4) C₆H₅ m.p.: 88° C. Cl

66 0 (2) — (4) C₆H₅ m.p.: 59° C. Cl

67 0 (2) (4) (3) CH₃ m.p.: 82° C. Cl SCH₃

68 0 (2) (4) (3) C₂H₅ m.p.: 64° C. Cl SC₂H₅

69 0 (2) (4) (3) CH₃ m.p.: 100° C. Cl SO₂CH₃

70 0 (2) (4) (3)

m.p.: 96° C. Cl SO₂CH₃

71 0 (4) — (2) C₆H₅ F

72 0 (4) — (2) C₆H₅ Cl

73 0 (4) — (2) C₆H₅ Br

74 0 (4) — (2) C₆H₅ I

75 0 (4) — (2) C₆H₅ CN

76 0 (4) — (2) C₆H₅ CF₃

77 0 (4) — (2) C₆H₅ CF₃

78 0 (2) (4) (3) C₆H₅ Cl Cl

79 0 (2) (4) (3) C₆H₅ Cl Cl

80 0 (2) (4) (3) C₆H₅ Cl Cl

81 0 (2) (4) (3) CH₃ Cl Cl

82 0 (2) (4) (3) CH₃ Cl Cl

83 0 (2) (4) (3) CH₃ Cl Cl

84 0 (2) (4) (3) C₂H₅ Cl Cl

85 0 (2) (4) (3) C₂H₅ Cl Cl

86 0 (2) (4) (3) C₂H₅ Cl Cl

87 0 (2) (4) (3) C₆H₅ Cl SO₂CH₃

88 0 (2) (4) (3) C₆H₅ Cl SO₂CH₃

89 0 (2) (4) (3) C₆H₅ Cl SO₂CH₃

90 0 (2) (4) (3) CH₃ Cl SO₂CH₃

91 0 (2) (4) (3) CH₃ Cl SO₂CH₃

92 0 (2) (4) (3) CH₃ Cl SO₂CH₃

93 0 (2) (4) (3) C₂H₅ Cl SO₂CH₃

94 0 (2) (4) (3) C₂H₅ Cl SO₂CH₃

95 0 (2) (4) (3) C₂H₅ Cl SO₂CH₃

96 0 (2) (4) (3) C₆H₅ m.p.: 94° C. Br Br

97 0 (2) (4) (3) C₆H₅ Br Br

98 0 (2) (4) (3) C₆H₅ m.p.: 86° C. Br Br

99 0 (2) (4) (3) CH₃ Br Br

100 0 (2) (4) (3) C₂H₅ Br Br

101 0 (2) (4) (3) C₆H₅ CH₃ SO₂CH₃

102 0 (2) (4) (3) C₆H₅ CH₃ SO₂CH₃

103 0 (2) (4) (3) C₆H₅ CH₃ SO₂CH₃

104 0 (2) (4) (3) CH₃ CH₃ SO₂CH₃

105 0 (2) (4) (3) C₂H₅ CH₃ SO₂CH₃

106 0 (2) (4) (3) C₆H₅ CH₃ SO₂CH₃

107 0 (2) (4) (3) C₆H₅ OCH₃ Cl

108 0 (2) (4) (3) C₆H₅ OCH₃ Cl

109 0 (2) (4) (3) CH₃ OCH₃ Cl

110 0 (2) (4) (3) C₂H₅ OCH₃ Cl

111 0 (2) — (4) C₆H₅ Br

112 0 (2) — (4) C₆H₅ I

113 0 (2) — (4) C₆H₅ CF₃

114 0 (2) — (4) C₆H₅ CN

115 0 (2) — (4) C₆H₅ NO₂

116 0 (2) — (4) C₆H₅ NO₂

117 0 (2) — (4) C₆H₅ NO₂

118 0 (2) — (4) CH₃ NO₂

119 0 (2) — (4) C₂H₅ NO₂

120 0 (2) (4) (3) C₆H₅ m.p.: 154° C. Cl Cl

logP = 4.02^(a)) 121 0 (2) (4) (3) C₆H₅ m.p.: 156° C. Cl Cl

logP = 3.98^(a)) 122 0 (2) (4) (3) C₆H₅ logP = 3.11^(a)) Cl SO₂CH₃

[0150] The logP values given in Table 1 were determined in accordance with EEC Directive 79/831 Annex V.A8 by HPLC (High Performance Liquid Chromatography) using a reversed-phase column (C 18). Temperature: 43° C.

[0151] (a) Mobile phases for the determination in the acidic range: 0.1% aqueous phosphoric acid, acetonitrile; linear gradient from 10% acetonitrile to 90% acetonitrile—the corresponding data are labelled ^(a)) in Table 1.

[0152] (b) Mobile phases for the determination in the neutral range: 0.01 molar aqueous phosphate buffer solution, acetonitrile; linear gradient from 10% acetonitrile to 90% acetonitrile—corresponding data are labelled ^(b)) in Table 1.

[0153] Calibration was carried out using unbranched alkan-2-ones (having 3 to 16 carbon atoms), with known logP values (determination of the logP values by the retention times using linear interpolation between two successive alkanones).

[0154] The lambda max values were determined in the maxima of the chromatographic signals, using the UV spectra from 200 nm to 400 nm. TABLE 2 Further examples of the compounds of the formula (I) (I)

Ex (position) (position) (position) (position) Physical No. n R¹, R2 R³ R⁴ —A-Z Y data 123 0 (4) CH₃, (2) (4) (3) C₆H₅ m.p.: (4) CH₃ Cl Cl

77° C. 124 0 (5) CH₃, (2) (4) (3) C₆H₅ m.p.: (5) CH₃ Cl Cl

85° C. 125 0 (4) CH₃, (2) (4) (3) C₆H₅ m.p.: (4) CH₃ Cl SO₂CH₃

99° C. 126 0 (5) CH₃, (2) (4) (3) C₆H₅ m.p.: (5) CH₃ Cl SO₂CH₃

104° C. 127 0 (3) (2) (4) (3) C₆H₅ m.p.: —CH₂CH₂—(5) Cl Cl

84° C. 128 0 (3) (4) — (2) C₆H₅ m.p.: —CH₂CH₂—(5) Br

186° C. 129 0 (3) (4) — (2) C₆H₅ m.p.: —CH₂CH₂—(5) CF₃

197° C. 130 0 (3) (2) — (4) C₆H₅ m.p.: —CH₂CH₂—(5) NO₂

84° C. 131 0 (3) (2) (4) (3) C₆H₅ —CH₂CH₂—(5) Cl Cl

132 0 (3) (2) (4) (3) C₆H₅ —CH₂CH₂—(5) Cl Cl

133 0 (3) (2) (4) (3) C₆H₅ —CH₂CH₂—(5) Cl Cl

134 0 (3) (2) (4) (3) C₆H₅ —CH₂CH₂—(5) Cl SO₂CH₃

135 0 (3) (2) (4) (3) C₆H₅ —CH₂CH₂—(5) Cl SO₂CH₃

136 0 (3) (2) (4) (3) C₆H₅ —CH₂CH₂—(5) Cl SO₂CH₃

137 0 (3) (2) (4) (3) CH₃ —CH₂CH₂—(5) Cl SO₂CH₃

138 0 (3) (2) (4) (3) C₂H₅ —CH₂CH₂—(5) Cl SO₂CH₃

139 0 (3) (2) (4) (3) C₆H₅ —CH₂CH₂—(5) Br Br

140 0 (3) (2) (4) (3) C₆H₅ —CH₂CH₂—(5) Br Br

141 0 (3) (2) (4) (3) C₆H₅ —CH₂CH₂—(5) CH₃ SO₂CH₃

142 0 (3) (2) (4) (3) C₆H₅ —CH₂CH₂—(5) CH₃ SO₂CH₃

143 0 (3) (2) (4) (3) C₆H₅ —CH₂CH₂—(5) OCH₃ Cl

144 0 (3) (2) (4) (3) C₆H₅ —CH₂CH₂—(5) OCH₃ Cl

USE EXAMPLES Example A

[0155] Pre-Emergence Test Solvent 5 parts by weight of acetone Emulsifier 1 part by weight of alkylaryl polyglycol ether

[0156] To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent, the stated amount of emulsifier is added and the concentrate is diluted with water to the desired concentration.

[0157] Seeds of the test plants are sown in normal soil. After 24 hours, the soil is sprayed with the preparation of active compound such that the particular amount of active compound desired is applied per unit area. The concentration of active compound in the spray liquor is chosen such that the particular amount of active compound desired is applied in 1000 litres of water per hectare.

[0158] After three weeks, the degree of damage to the plants is rated in % damage in comparison to the development of the untreated control. The figures denote:

[0159] 0%=no effect (like untreated control)

[0160] 100%=total destruction

[0161] In this test, for example, the compound of the Preparation Example 16 exhibits strong activity against weeds, and is tolerated well by some crop plants, such as, for example, maize.

Example B

[0162] Post-Emergence Test Solvent 5 parts by weight of acetone Emulsifier 1 part by weight of alkylaryl polyglycol ether

[0163] To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent, the stated amount of emulsifier is added and the concentrate is diluted with water to the desired concentration.

[0164] Test plants of a height of 5-15 cm are sprayed with the preparation of active compound such that the particular amounts of active compound desired are applied per unit area. The concentration of the spray liquor is chosen such that the particular amounts of active compound desired are applied in 1000 l of water/ha.

[0165] After three weeks, the degree of damage to the plants is rated in % damage in comparison to the development of the untreated control.

[0166] The figures denote:

[0167] 0%=no effect (like untreated control)

[0168] 100%=total destruction

[0169] In this test, for example, the compounds of Preparation Examples 1, 2, 5, 16, 17, 18, 19 and 20 exhibit strong activity against weeds, and they are tolerated well by some crop plants, such as, for example, maize and wheat. 

1. Substituted benzoylcyclohexenones of the formula (I),

in which n represents the number 0, 1 or 2, A represents a single bond or represents alkanediyl (alkylene) having 1 to 6 carbon atoms, R¹ represents hydrogen, phenyl or optionally cyano-, halogen-, C₁-C₄-alkoxy- or C₁-C₄-alkylthio-substituted alkyl having 1 to 6 carbon atoms, R² represents hydrogen or optionally cyano-, halogen-, C₁-C₄-alkoxy- or C₁-C₄-alkylthio-substituted alkyl having 1 to 6 carbon atoms, or together with R¹ represents alkanediyl (alkylene) having 1 to 6 carbon atoms, or together with R¹—in this case attached to the same carbon atom—and the carbon atom to which R¹ and R² are attached in this case represents a (C═O) grouping, R³ represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, halogen, or represents in each case optionally cyano-, halogen- or C₁-C₄-alkoxy-substituted alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, alkylamino, dialkylamino or dialkylaminosulphonyl having in each case 1 to 6 carbon atoms in the alkyl groups, R⁴ represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, halogen, or represents in each case optionally cyano-, halogen- or C₁-C₄-alkoxy-substituted alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, alkylamino, dialkylamino or dialkylaminosulphonyl having in each case 1 to 6 carbon atoms in the alkyl groups, and Y represents hydrogen, represents optionally cyano-, halogen- or C₁-C₄-alkoxy-substituted alkyl having 1 to 10 carbon atoms, represents in each case optionally cyano-, halogen-, C₁-C₄-alkyl-carbonyl- or C₁-C₄-alkoxy-carbonyl-substituted alkenyl or alkinyl having in each case 2 to 10 carbon atoms, or represents in each case optionally nitro-, amino-, cyano-, carboxyl-, carbamoyl-, thiocarbamoyl-, halogen-, C₁-C₄-alkyl-, C₁-C₄-halogenoalkyl-, C₁-C₄-alkoxy-C₁-C₄-alkyl-, C₁-C₄-alkoxy-, C₁-C₄-halogenoalkoxy-, C₁-C₄-alkylthio-, C₁-C₄-halogenoalkylthio-, C₁-C₄-alkylsulphinyl-, C₁-C₄-halogenoalkylsulphinyl-, C₁-C₄-alkylsulphonyl-, C₁-C₄-halogenoalkylsulphonyl-, C₁-C₄-alkyl-carbonyl-, C₁-C₄-alkoxy-carbonyl-, C₁-C₄-alkyl-carbonyl-amino-, C₁-C₄-alkoxy-carbonyl-amino-, C₁-C₄-alkyl-sulphonyl-amino-substituted aryl or arylalkyl having in each case 6 or 10 carbon atoms in the aryl groups and optionally 1 to 4 carbon atoms in the alkyl moiety, and Z represents an optionally substituted 4- to 12-membered saturated or unsaturated, monocyclic or bicyclic, heterocyclic grouping which contains 1 to 4 hetero atoms (up to 4 nitrogen atoms and optionally—alternatively or additionally—one oxygen atom or one sulphur atom, or one SO grouping or one SO₂ grouping), and which contains additionally one to three oxo groups (C═O) and/or thioxo groups (C═S) as components of the heterocycle, including all possible tautomeric and, if appropriate, possible stereoisomeric forms of the compounds of the general formula (I), and the possible salts or metal-coordinated derivatives of the compounds of the formula (I).
 2. Compounds according to claim 1, characterized in that n represents the number 0 or 2, A represents a single bond or represents alkanediyl (alkylene) having 1 to 4 carbon atoms, R¹ represents hydrogen, phenyl or optionally cyano-, halogen-, C₁-C₄-alkoxy- or C₁-C₄-alkylthio-substituted alkyl having 1 to 5 carbon atoms, R² represents hydrogen or optionally cyano-, halogen-, C₁-C₄-alkoxy- or C₁-C₄-alkylthio-substituted alkyl having 1 to 5 carbon atoms, or together with R¹ represents alkanediyl (alkylene) having 1 to 5 carbon atoms, R³ represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, halogen, or represents in each case optionally cyano-, halogen- or C₁-C₄-alkoxy-substituted alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, alkylamino, dialkylamino or dialkylaminosulphonyl having in each case 1 to 5 carbon atoms in the alkyl groups, R⁴ represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, halogen, or represents in each case optionally cyano-, halogen- or C₁-C₄-alkoxy-substituted alkyl, alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, alkylamino, dialkylamino or dialkylaminosulphonyl having in each case 1 to 5 carbon atoms in the alkyl groups, Y represents hydrogen, represents optionally cyano-, halogen- or C₁-C₄-alkoxy-substituted alkyl having 1 to 6 carbon atoms, represents in each case optionally cyano-, halogen-, C₁-C₄-alkyl-carbonyl- or C₁-C₄-alkoxy-carbonyl-substituted alkenyl or alkinyl having in each case 2 to 6 carbon atoms, or represents in each case optionally nitro-, amino-, cyano-, carboxyl-, carbamoyl-, thiocarbamoyl-, halogen-, C₁-C₄-alkyl-, C₁-C₄-halogenoalkyl-, C₁-C₄-alkoxy-C₁-C₄-alkyl-, C₁-C₄-alkoxy-, C₁-C₄-halogenoalkoxy-, C₁-C₄-alkylthio, C₁-C₄-halogenoalkylthio-, C₁-C₄-alkylsulphinyl-, C₁-C₄-halogenoalkylsulphinyl-, C₁-C₄-alkylsulphonyl-, C₁-C₄-halogenoalkylsulphonyl-, C₁-C₄-alkyl-carbonyl-, C₁-C₄-alkoxy-carbonyl-, C₁-C₄-alkyl-carbonyl-amino-, C₁-C₄-alkoxy-carbonyl-amino-, C₁-C₄-alkyl-sulphonyl-amino-substituted aryl or arylalkyl having in each case 6 or 10 carbon atoms in the aryl groups and optionally 1 to 4 carbon atoms in the alkyl moiety, Z represents one of the heterocyclic groupings below

in which the bond drawn broken in each case denotes a single bond or a double bond, and in which each heterocycle preferably only carries two substituents of the definition R⁵ and/or R⁶ in any combination, Q represents oxygen or sulphur, R⁵ represents hydrogen, hydroxyl, mercapto, cyano, halogen, represents in each case optionally cyano-, halogen-, C₁-C₄-alkoxy-, C₁-C₄-alkylthio-, C₁-C₄-alkylsulphinyl- or C₁-C₄-alkylsulphonyl-substituted alkyl, alkylcarbonyl, alkoxy, alkoxycarbonyl, alkylthio, alkylsulphinyl or alkylsulphonyl having in each case up to 6 carbon atoms in the alkyl groups, represents in each case optionally halogen-substituted alkylamino or dialkylamino having in each case up to 6 carbon atoms in the alkyl groups, represents in each case optionally halogen-substituted alkenyl, alkinyl, alkenyloxy, alkenylthio, aikinylthio or alkenylamino having in each case up to 6 carbon atoms in the alkenyl or alkinyl groups, represents in each case optionally halogen-substituted cycloalkyl, cycloalkyloxy, cycloalkylthio, cycloalkylamino, cycloalkylalkyl, cycloalkylalkoxy, cycloalkylalkylthio or cycloalkylalkylamino having in each case 3 to 6 carbon atoms in the cycloalkyl groups and optionally up to 4 carbon atoms in the alkyl moiety, or represents in each case optionally halogen-, C₁-C₄-alkyl- or C₁-C₄-alkoxy-substituted phenyl, phenyloxy, phenylthio, phenylamino, benzyl, benzyloxy, benzylthio or benzylamino, represents pyrrolidino, piperidino or morpholino, or—if two adjacent radicals R⁵ and R⁵ are located at a double bond—also together with the adjacent radical R⁵ represents a benzo grouping, and R⁶ represents hydrogen, hydroxyl, amino, alkylideneamino having up to 4 carbon atoms, represents in each case optionally halogen- or C₁-C₄-alkoxy-substituted alkyl, alkoxy, alkylamino, dialkylamino or alkanoylamino having in each case up to 6 carbon atoms in the alkyl groups, represents in each case optionally halogen-substituted alkenyl, alkinyl or alkenyloxy having in each case up to 6 carbon atoms in the alkenyl or alkinyl groups, represents in each case optionally halogen-substituted cycloalkyl, cycloalkylalkyl or cycloalkylamino having in each case 3 to 6 carbon atoms in the cycloalkyl groups and optionally up to 3 carbon atoms in the alkyl moiety, or represents in each case optionally halogen-, C₁-C₄-alkyl- or C₁-C₄-alkoxy-substituted phenyl or benzyl, or together with an adjacent radical R or R⁶ represents optionally halogen- or C₁-C₄-alkyl-substituted alkanedjyl having 3 to 5 carbon atoms, where the individual radicals R⁵ and R⁶—if two or more of them are attached to the same heterocyclic groupings—may have identical or different meanings in the context of the above definition.
 3. Compounds according to claim 1 or 2, characterized in that A represents a single bond or represents methylene, ethylidene (ethane-1,1-diyl) or dimethylene (ethane-1,2-diyl), R¹ represents hydrogen, phenyl or in each case optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-, methylthio-, ethylthio-, n- or i-propylthio-substituted methyl, ethyl, n- or i-propyl, n-, 1- or s-butyl, R² represents hydrogen or represents in each case optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-, methylthio-, ethylthio-, n- or i-propylthio-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, or together with R¹ represents methylene, ethylidene (ethane-1,1-diyl), dimethylene (ethane-1,2-diyl), propylidene (propane-1,1-diyl) or trimethylene (propane-1,3-diyl), R³ represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, fluorine, chlorine, bromine, iodine, or represents in each case optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methylthio, ethylthio, n- or i-propylthio, n-, i-, s- or t-butylthio, methylsulphinyl, ethylsulphinyl, n- or i-propylsulphinyl, methylsulphonyl, ethylsulphonyl, n- or i-propylsulphonyl, methylamino, ethylamino, n- or i-propylamino, n-, i-, s- or t-butylamino, dimethylamino, diethylamino, dimethylaminosulphonyl or diethylaminosulphonyl, R⁴ represents hydrogen, nitro, cyano, carboxyl, carbamoyl, thiocarbamoyl, fluorine, chlorine, bromine, iodine, or represents in each case optionally cyano-, fluonrne-, chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methylthio, ethylthio, n- or i-propylthio, n-, i-, s- or t-butylthio, methylsulphinyl, ethylsulphinyl, n- or i-propylsulphinyl, methylsulphonyl, ethylsulphonyl, n- or i-propylsulphonyl, methylamino, ethylamino, n- or i-propylamino, n-, i-, s- or t-butylamino, dimethylamino, diethylamino, dimethylaminosulphonyl or diethylaminosulphonyl, Y represents hydrogen, represents in each case optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, represents in each case optionally cyano-, fluorine-, chlorine-, bromine-, acetyl-, propionyl-, n- or i-butyroyl-, methoxycarbonyl-, ethoxycarbonyl-, n- or i-propoxycarbonyl-substituted ethenyl, propenyl, butenyl, pentenyl, ethinyl, propinyl or butinyl, or represents in each case optionally nitro-, amino-, cyano-, carboxyl-, carbamoyl-, thiocarbamoyl-, fluorine-, chlorine-, bromine-, iodine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-, trifluoromethyl-, methoxymethyl-, ethoxymethyl-, methoxyethyl-, ethoxyethyl-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s- or t-butoxy-, difluoromethoxy-, trifluoromethoxy-, methylthio-, ethylthio-, n- or i-propylthio-, n-, i-, s- or t-butylthio-, difluoromethylthio-, trifluoromethylthio-, methylsulphinyl-, ethylsulphinyl-, trifluoromethylsulphinyl-, methylsulphonyl-, ethylsulphonyl-, trifluoromethylsulphonyl-, acetyl-, propionyl-, n- or i-butyroyl-, methoxycarbonyl-, ethoxycarbonyl-, n- or i-propoxycarbonyl-, acetylamino-, propionylamino-, methoxycarbonylamino-, ethoxycarbonylamino-, methylsulphonylamino-, ethylsulphonylamino-, n- or i-propylsulphonylamino-substituted phenyl, naphthyl, benzyl or phenylethyl, Z represents one of the heterocyclic groupings below

Q represents oxygen, R⁵ represents hydrogen, hydroxyl, mercapto, cyano, fluorine, chlorine, bromine, iodine, represents in each case optionally fluorine-, chlorine-, methoxy-, ethoxy-, n- or i-propoxy-, n-, i-, s- or t-butoxy-, methylthio-, ethylthio-, n- or i-propylthio-, n-, i-, s- or t-butylthio-, methylsulphinyl-, ethylsulphinyl-, n- or i-propylsulphinyl-, methylsulphonyl-, ethylsulphonyl-, n- or i-propylsulphonyl-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, methoxy, ethoxy, n- or i-propoxy, n-, i-, s- or t-butoxy, methylthio, ethylthio, n- or i-propylthio, n-, i-, s- or t-butylthio, methylsulphinyl, ethylsulphinyl, n- or i-propylsulphinyl, methylsulphonyl, ethylsulphonyl, n- or i-propylsulphonyl, represents methylamino, ethylamino, n- or i-propylamino, n-, i-, s- or t-butylamino, dimethylamino, diethylamino, di-n-propylamino or di-i-propylamino, represents in each case optionally fluorine- and/or chlorine-substituted ethenyl, propenyl, butenyl, ethinyl, propinyl, butinyl, propenyloxy, butenyloxy, propenylthio, butenylthio, propenylamino or butenylamino, represents in each case optionally fluorine- and/or chlorine-substituted cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cyclopropylthio, cyclobutylthio, cyclopentylthio, cyclohexylthio, cyclopropylamino, cyclobutylamino, cyclopentylamino, cyclohexylamino, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, cyclopropylmethoxy, cyclobutylmethoxy, cyclopentylmethoxy, cyclohexylmethoxy, cyclopropylmethylthio, cyclobutylmethylthio, cyclopentylmethylthio, cyclohexylmethylthio, cyclopropylmethylamino, cyclobutylmethylamino, cyclopentylmethylamino or cyclohexylmethylamino, or represents in each case optionally fluorine-, chlorine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-, methoxy-, ethoxy-, n- or i-propoxy-substituted phenyl, phenyloxy, phenylthio, phenylamino, benzyl, benzyloxy, benzylthio or benzylamino, or—in the case that two adjacent radicals R⁵ and R⁵ are located at a double bond—together with the adjacent radical R⁵ also represents a benzo grouping, and R⁶ represents hydrogen, hydroxyl, amino, represents in each case optionally fluorine- and/or chlorine-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, methoxy, ethoxy, n- or i-propoxy, methylamino, ethylamino or dimethylamino, represents in each case optionally fluorine- and/or chlorine-substituted ethenyl, propenyl, ethinyl, propinyl or propenyloxy, represents in each case optionally fluorine- and/or chlorine-substituted cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl or cyclohexylmethyl, or represents in each case optionally fluorine-, chlorine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-, methoxy-, ethoxy-, n- or i-propoxy-substituted phenyl or benzyl, or together with an adjacent radical R⁵ or R⁶ represents in each case optionally methyl- and/or ethyl-substituted propane-1,3-diyl (trimethylene), butane-1,4-diyl (tetramethylene) or pentane-1,5-diyl (pentamethylene).
 4. Compounds according to any of claims 1 to 3, characterized in that A represents a single bond or represents methylene, R¹ represents hydrogen, phenyl or in each case optionally fluorine- or chlorine-substituted methyl, ethyl, n- or i-propyl, R² represents hydrogen or in each case optionally fluorine- or chlorine-substituted methyl, ethyl, n- or i-propyl, or together with R¹ represents methylene or dimethylene, R³ represents hydrogen, nitro, cyano, fluorine, chlorine, bromine, iodine, or represents in each case optionally fluorine-, chlorine-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, methoxy, ethoxy, methylthio, ethylthio, methylsulphinyl, ethylsulphinyl, methylsulphonyl, ethylsulphonyl, methylamino, ethylamino, dimethylamino or dimethylaminosulphonyl, R⁴ represents hydrogen, nitro, cyano, fluorine, chlorine, bromine, iodine, or represents in each case optionally fluorine-, chlorine-, methoxy- or ethoxy-substituted methyl, ethyl, n- or i-propyl, methoxy, ethoxy, methylthio, ethylthio, methylsulphinyl, ethylsulphinyl, methylsulphonyl, ethylsulphonyl, methylamino, ethylamino, dimethylamino or dimethylaminosulphonyl, Y represents hydrogen, represents in each case optionally cyano-, fluorine-, chlorine-, bromine-, methoxy-, ethoxy-, n- or i-propoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, represents in each case optionally fluorine-, chlorine- or bromine-substituted propenyl, butenyl, pentenyl, propinyl or butinyl, or represents in each case optionally nitro-, amino-, cyano-, fluorine-, chlorine-, bromine-, methyl-, ethyl-, n- or i-propyl-, n-, i-, s- or t-butyl-, trifluoromethyl-, methoxymethyl-, ethoxymethyl-, methoxyethyl-, ethoxyethyl-, methoxy-, ethoxy-, n- or i-propoxy-, difluoromethoxy-, trifluoromethoxy-, methylthio-, ethylthio-, n- or i-propylthio-, difluoromethylthio-, trifluoromethylthio-, methylsulphinyl-, ethylsulphinyl-, trifluoromethylsulphinyl-, methylsulphonyl, ethylsulphonyl-, trifluoromethylsulphonyl-, acetyl-, propionyl-, methoxycarbonyl-, ethoxycarbonyl-, acetylamino-, propionylamino-, methoxycarbonylamino-, ethoxycarbonylamino-, methylsulphonylamino- or ethylsulphonylamino-substituted phenyl or benzyl, R⁵ represents hydrogen, fluorine, chlorine, bromine, represents in each case optionally fluorine-, chlorine-, methoxy-, ethoxy-, n- or 1-propoxy-, methylthio-, ethylthio-, methylsulphinyl-, ethylsulphinyl-, methylsulphonyl-, ethylsulphonyl-substituted methyl, ethyl, n- or i-propyl, n-, i- or s-butyl, methoxy, ethoxy, n- or i-propoxy, n-, i- or s-butoxy, methylthio, ethylthio, n- or i-propylthio, n-, i- or s-butylthio, methylsulphinyl, ethylsulphinyl, n- or i-propylsulphinyl, methylsulphonyl, ethylsulphonyl, n- or i-propylsulphonyl, represents methylamino, ethylamino, n- or i-propylamino, n-, i- or s-butylamino, dimethylamino or diethylamino, represents in each case optionally fluorine- and/or chlorine-substituted ethenyl, propenyl, butenyl, ethinyl, propinyl, butinyl, propenyloxy, butenyloxy, propenylthio or represents in each case optionally fluorine- and/or chlorine-substituted cyclopropyl, cyclopropyloxy, cyclopropylthio, cyclopropylamino, cyclopropylmnethyl, cyclopropylmethoxy, cyclopropylmethylthio or cyclopropylmethylamino, and R⁶ represents hydrogen, represents amino, represents in each case optionally fluorine- and/or chlorine-, methoxy- or ethoxy-substituted methyl, ethyl, methoxy, ethoxy, methylamino or ethylamino, represents dimethylamino, or represents in each case optionally fluorine- and/or chlorine-substituted cyclopropyl, cyclopropylmethyl, phenyl or benzyl, or together with an adjacent radical R or R⁶ represents in each case optionally methyl- and/or ethyl-substituted propane-1,3-diyl (trimethylene), butane-1,4-diyl (tetramethylene) or pentane-1,5-diyl (pentamethylene).
 5. Compounds according to any of claims 1 to 4, characterized in that R¹ represents hydrogen, R² represents hydrogen, R³ represents chlorine, trifluoromethyl or methoxy, R⁴ represents chlorine, trifluoromethyl or methylsulphonyl, R⁵ represents hydrogen, methyl or ethyl, and R⁶ represents hydrogen, methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, cyclopropyl, cyclopropylmethyl, cyclopentyl, cyclopentylmethyl, cyclohexyl, cyclohexylmethyl, phenyl or benzyl.
 6. Compounds according to any of claims 1 to 5, characterized in that R⁵ represents hydrogen, and R⁶ represents methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, cyclopropyl, cyclopropylmethyl or phenyl.
 7. Compounds according to any of claims 1 to 6, characterized in that n represents the number
 0. 8. Compounds according to any of claims 1 to 7, characterized in that Z represents one of the groupings below


9. Compounds according to any of claims 1 to 8, characterized in that Q represents oxygen.
 10. Compounds according to any of claims 1 to 9, characterized in that Y represents hydrogen, represents in each case optionally fluorine-, chlorine- or methoxy-substituted methyl, ethyl, n- or i-propyl, n-, i-, s- or t-butyl, represents in each case optionally fluorine- or chlorine-substituted propenyl, butenyl, pentenyl or represents optionally amino-, cyano-, fluorine-, chlorine-, methyl-, ethyl-, trifluoromethyl-, methoxy- or ethoxy-substituted phenyl.
 11. Compounds of the formula (IA)

in which n, A, R¹, R², R³, R⁴, Y and Z are as defined in any of claims 1 to
 9. 12. Compounds of the formula (IB)

in which n, A, R¹, R², R³, R⁴, Y and Z are as defined in any of claims 1 to
 9. 13. Compounds of the formula (IC)

in which n, A, R¹, R², R³, R⁴, Y and Z are as defined in any of claims 1 to
 9. 14. Sodium, potassium, magnesium, calcium, ammonium, C₁-C₄-alkyl-ammonium, di-(C₁-C₄-alkyl)-ammonium, tri-(C₁-C₄-alkyl)-ammonium-, tetra-(C₁-C₄-alkyl)-ammonium, tri-(C₁-C₄-alkyl)-sulphonium, C₅- or C₆-cycloalkyl-ammonium and di-(C₁-C₂-alkyl)-benzyl-ammonium salts of compounds of the formula (I) according to any of claims 1 to 13, and their complex compounds with metals such as copper, iron, cobalt, nickel.
 15. Process for preparing compounds according to any of claims 1 to 12, characterized in that compounds of the formula (II)

in which A, R¹, R², R³, R⁴ and Z are as defined in any of claims 1 to 9 are reacted with a halogenating agent, if appropriate in the presence of a reaction auxiliary and if appropriate in the presence of a diluent, and the halogenocyclohexenones obtained in this way (in the first reaction step), of the formula (III)

in which A, R¹, R², R³, R⁴ and Z are as defined in any of claims 1 to 9 and X represents halogen after intermediate isolation or without intermediate isolation (“in situ”) are reacted in a second reaction step with mercapto compounds of the formula (IV) HS—Y  (IV) in which Y is as defined above, if appropriate in the presence of a reaction auxiliary and if appropriate in the presence of a diluent, and, if appropriate, the compounds of the formula (I) obtained in this manner are subsequently subjected in a customary manner, within the scope of the definition of the substituents, to electrophilic or nucleophilic substitution reactions or oxidation or reduction reactions, or the compounds of the formula (I) are converted in a customary manner into salts.
 16. Herbicidal compositions, characterized in that they comprise at least one compound according to any of claims 1 to 12 and customary extenders.
 17. Use of at least one compound according to any of claims 1 to 12 for controlling undesirable plants.
 18. Method for controlling undesirable plants, characterized in that at least one compound according to any of claims 1 to 13 or a composition according to claim 16 is allowed to act on the undesirable plants and/or their habitat. 